U.S. flag

An official website of the United States government

nsv7098706

  • Variant Calls:40
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 97 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):105,488,273-105,488,273Question Mark
    Overlapping variant regions from other studies: 97 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):105,488,274-105,488,274Question Mark
    Overlapping variant regions from other studies: 87 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):105,962,240-105,962,240Question Mark
    Overlapping variant regions from other studies: 87 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):105,962,240-105,962,240Question Mark
    Overlapping variant regions from other studies: 94 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):106,108,623-106,108,623Question Mark
    Overlapping variant regions from other studies: 94 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):106,108,624-106,108,624Question Mark
    Overlapping variant regions from other studies: 91 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):106,830,619-106,830,619Question Mark
    Overlapping variant regions from other studies: 91 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):106,830,620-106,830,620Question Mark
    Overlapping variant regions from other studies: 99 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):107,706,152-107,706,152Question Mark
    Overlapping variant regions from other studies: 99 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):107,706,155-107,706,155Question Mark
    Overlapping variant regions from other studies: 121 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):108,651,910-108,651,910Question Mark
    Overlapping variant regions from other studies: 121 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):108,651,916-108,651,916Question Mark
    Overlapping variant regions from other studies: 158 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):109,096,778-109,096,778Question Mark
    Overlapping variant regions from other studies: 158 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):109,097,268-109,097,268Question Mark
    Overlapping variant regions from other studies: 110 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):120,208,269-120,208,269Question Mark
    Overlapping variant regions from other studies: 110 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):120,208,275-120,208,275Question Mark
    Overlapping variant regions from other studies: 112 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):154,775,336-154,775,336Question Mark
    Overlapping variant regions from other studies: 112 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):154,775,345-154,775,345Question Mark
    Overlapping variant regions from other studies: 121 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):154,833,957-154,833,957Question Mark
    Overlapping variant regions from other studies: 121 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):154,833,959-154,833,959Question Mark
    Overlapping variant regions from other studies: 118 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):154,836,803-154,836,803Question Mark
    Overlapping variant regions from other studies: 118 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):154,836,815-154,836,815Question Mark
    Overlapping variant regions from other studies: 127 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):155,027,218-155,027,218Question Mark
    Overlapping variant regions from other studies: 127 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):155,027,227-155,027,227Question Mark
    Overlapping variant regions from other studies: 113 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):156,107,069-156,107,069Question Mark
    Overlapping variant regions from other studies: 113 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):156,107,070-156,107,070Question Mark
    Overlapping variant regions from other studies: 159 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):83,070,804-83,070,804Question Mark
    Overlapping variant regions from other studies: 159 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):83,070,806-83,070,806Question Mark
    Overlapping variant regions from other studies: 175 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):83,098,726-83,098,726Question Mark
    Overlapping variant regions from other studies: 175 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):83,098,794-83,098,794Question Mark
    Overlapping variant regions from other studies: 174 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):83,098,946-83,098,946Question Mark
    Overlapping variant regions from other studies: 174 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):83,098,955-83,098,955Question Mark
    Overlapping variant regions from other studies: 175 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):83,126,417-83,126,417Question Mark
    Overlapping variant regions from other studies: 175 SVs from 35 studies. See in: genome view    
    Remapped(Score: Perfect):83,126,420-83,126,420Question Mark
    Overlapping variant regions from other studies: 130 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):83,673,107-83,673,107Question Mark
    Overlapping variant regions from other studies: 130 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):83,673,107-83,673,107Question Mark
    Overlapping variant regions from other studies: 134 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):84,151,110-84,151,110Question Mark
    Overlapping variant regions from other studies: 134 SVs from 29 studies. See in: genome view    
    Remapped(Score: Perfect):84,151,111-84,151,111Question Mark
    Overlapping variant regions from other studies: 135 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):84,289,378-84,289,378Question Mark
    Overlapping variant regions from other studies: 135 SVs from 33 studies. See in: genome view    
    Remapped(Score: Perfect):84,289,380-84,289,380Question Mark
    Overlapping variant regions from other studies: 140 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):84,461,358-84,461,358Question Mark
    Overlapping variant regions from other studies: 140 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):84,461,360-84,461,360Question Mark
    Overlapping variant regions from other studies: 122 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):84,857,787-84,857,787Question Mark
    Overlapping variant regions from other studies: 122 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):84,857,802-84,857,802Question Mark
    Overlapping variant regions from other studies: 101 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):85,028,643-85,028,643Question Mark
    Overlapping variant regions from other studies: 101 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):85,028,649-85,028,649Question Mark
    Overlapping variant regions from other studies: 126 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):85,147,879-85,147,879Question Mark
    Overlapping variant regions from other studies: 126 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):85,147,902-85,147,902Question Mark
    Overlapping variant regions from other studies: 126 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):85,147,916-85,147,916Question Mark
    Overlapping variant regions from other studies: 126 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):85,147,917-85,147,917Question Mark
    Overlapping variant regions from other studies: 95 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):85,839,006-85,839,006Question Mark
    Overlapping variant regions from other studies: 95 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):85,839,008-85,839,008Question Mark
    Overlapping variant regions from other studies: 97 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):85,885,258-85,885,258Question Mark
    Overlapping variant regions from other studies: 97 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):85,885,261-85,885,261Question Mark
    Overlapping variant regions from other studies: 102 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):85,933,827-85,933,827Question Mark
    Overlapping variant regions from other studies: 102 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):85,933,827-85,933,827Question Mark
    Overlapping variant regions from other studies: 87 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):86,168,535-86,168,535Question Mark
    Overlapping variant regions from other studies: 87 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):86,168,535-86,168,535Question Mark
    Overlapping variant regions from other studies: 88 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):86,448,458-86,448,458Question Mark
    Overlapping variant regions from other studies: 88 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):86,448,466-86,448,466Question Mark
    Overlapping variant regions from other studies: 173 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):108,522,752-108,522,752Question Mark
    Overlapping variant regions from other studies: 173 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):108,522,762-108,522,762Question Mark
    Overlapping variant regions from other studies: 173 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):108,523,003-108,523,003Question Mark
    Overlapping variant regions from other studies: 173 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):108,523,020-108,523,020Question Mark
    Overlapping variant regions from other studies: 162 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):83,064,128-83,064,128Question Mark
    Overlapping variant regions from other studies: 162 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):83,064,779-83,064,779Question Mark
    Overlapping variant regions from other studies: 168 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):83,624,728-83,624,728Question Mark
    Overlapping variant regions from other studies: 168 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):83,624,730-83,624,730Question Mark
    Overlapping variant regions from other studies: 160 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):83,652,590-83,652,590Question Mark
    Overlapping variant regions from other studies: 160 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):83,652,595-83,652,595Question Mark
    Overlapping variant regions from other studies: 157 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):83,817,478-83,817,478Question Mark
    Overlapping variant regions from other studies: 157 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):83,817,482-83,817,482Question Mark
    Overlapping variant regions from other studies: 157 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):83,827,097-83,827,097Question Mark
    Overlapping variant regions from other studies: 157 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):83,827,097-83,827,097Question Mark
    Overlapping variant regions from other studies: 155 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):83,877,111-83,877,111Question Mark
    Overlapping variant regions from other studies: 155 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):83,877,111-83,877,111Question Mark
    Overlapping variant regions from other studies: 88 SVs from 14 studies. See in: genome view    
    Remapped(Score: Perfect):19,039,800-19,039,800Question Mark
    Overlapping variant regions from other studies: 88 SVs from 14 studies. See in: genome view    
    Remapped(Score: Perfect):19,039,802-19,039,802Question Mark
    Overlapping variant regions from other studies: 131 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):37,920,655-37,920,655Question Mark
    Overlapping variant regions from other studies: 131 SVs from 20 studies. See in: genome view    
    Remapped(Score: Perfect):37,920,655-37,920,655Question Mark
    Overlapping variant regions from other studies: 13 SVs from 9 studies. See in: genome view    
    Remapped(Score: Perfect):57,820-57,820Question Mark
    Overlapping variant regions from other studies: 13 SVs from 9 studies. See in: genome view    
    Remapped(Score: Perfect):57,835-57,835Question Mark
    Overlapping variant regions from other studies: 97 SVs from 22 studies. See in: genome view    
    Submitted genomic105,207,117-105,207,117Question Mark
    Overlapping variant regions from other studies: 97 SVs from 22 studies. See in: genome view    
    Submitted genomic105,207,118-105,207,118Question Mark
    Overlapping variant regions from other studies: 87 SVs from 19 studies. See in: genome view    
    Submitted genomic105,681,087-105,681,087Question Mark
    Overlapping variant regions from other studies: 87 SVs from 19 studies. See in: genome view    
    Submitted genomic105,681,087-105,681,087Question Mark
    Overlapping variant regions from other studies: 94 SVs from 21 studies. See in: genome view    
    Submitted genomic105,827,470-105,827,470Question Mark
    Overlapping variant regions from other studies: 94 SVs from 21 studies. See in: genome view    
    Submitted genomic105,827,471-105,827,471Question Mark
    Overlapping variant regions from other studies: 91 SVs from 20 studies. See in: genome view    
    Submitted genomic106,549,466-106,549,466Question Mark
    Overlapping variant regions from other studies: 91 SVs from 20 studies. See in: genome view    
    Submitted genomic106,549,467-106,549,467Question Mark
    Overlapping variant regions from other studies: 99 SVs from 22 studies. See in: genome view    
    Submitted genomic107,424,999-107,424,999Question Mark
    Overlapping variant regions from other studies: 99 SVs from 22 studies. See in: genome view    
    Submitted genomic107,425,002-107,425,002Question Mark
    Overlapping variant regions from other studies: 121 SVs from 25 studies. See in: genome view    
    Submitted genomic108,370,757-108,370,757Question Mark
    Overlapping variant regions from other studies: 121 SVs from 25 studies. See in: genome view    
    Submitted genomic108,370,763-108,370,763Question Mark
    Overlapping variant regions from other studies: 158 SVs from 33 studies. See in: genome view    
    Submitted genomic108,815,625-108,815,625Question Mark
    Overlapping variant regions from other studies: 158 SVs from 33 studies. See in: genome view    
    Submitted genomic108,816,115-108,816,115Question Mark
    Overlapping variant regions from other studies: 110 SVs from 18 studies. See in: genome view    
    Submitted genomic119,927,116-119,927,116Question Mark
    Overlapping variant regions from other studies: 110 SVs from 18 studies. See in: genome view    
    Submitted genomic119,927,122-119,927,122Question Mark
    Overlapping variant regions from other studies: 112 SVs from 22 studies. See in: genome view    
    Submitted genomic154,493,125-154,493,125Question Mark
    Overlapping variant regions from other studies: 112 SVs from 22 studies. See in: genome view    
    Submitted genomic154,493,134-154,493,134Question Mark
    Overlapping variant regions from other studies: 121 SVs from 24 studies. See in: genome view    
    Submitted genomic154,551,746-154,551,746Question Mark
    Overlapping variant regions from other studies: 121 SVs from 24 studies. See in: genome view    
    Submitted genomic154,551,748-154,551,748Question Mark
    Overlapping variant regions from other studies: 118 SVs from 25 studies. See in: genome view    
    Submitted genomic154,554,592-154,554,592Question Mark
    Overlapping variant regions from other studies: 118 SVs from 25 studies. See in: genome view    
    Submitted genomic154,554,604-154,554,604Question Mark
    Overlapping variant regions from other studies: 127 SVs from 23 studies. See in: genome view    
    Submitted genomic154,745,007-154,745,007Question Mark
    Overlapping variant regions from other studies: 127 SVs from 23 studies. See in: genome view    
    Submitted genomic154,745,016-154,745,016Question Mark
    Overlapping variant regions from other studies: 113 SVs from 18 studies. See in: genome view    
    Submitted genomic155,824,858-155,824,858Question Mark
    Overlapping variant regions from other studies: 113 SVs from 18 studies. See in: genome view    
    Submitted genomic155,824,859-155,824,859Question Mark
    Overlapping variant regions from other studies: 159 SVs from 33 studies. See in: genome view    
    Submitted genomic83,119,955-83,119,955Question Mark
    Overlapping variant regions from other studies: 159 SVs from 33 studies. See in: genome view    
    Submitted genomic83,119,957-83,119,957Question Mark
    Overlapping variant regions from other studies: 175 SVs from 35 studies. See in: genome view    
    Submitted genomic83,147,877-83,147,877Question Mark
    Overlapping variant regions from other studies: 175 SVs from 35 studies. See in: genome view    
    Submitted genomic83,147,945-83,147,945Question Mark
    Overlapping variant regions from other studies: 174 SVs from 35 studies. See in: genome view    
    Submitted genomic83,148,097-83,148,097Question Mark
    Overlapping variant regions from other studies: 174 SVs from 35 studies. See in: genome view    
    Submitted genomic83,148,106-83,148,106Question Mark
    Overlapping variant regions from other studies: 175 SVs from 35 studies. See in: genome view    
    Submitted genomic83,175,568-83,175,568Question Mark
    Overlapping variant regions from other studies: 175 SVs from 35 studies. See in: genome view    
    Submitted genomic83,175,571-83,175,571Question Mark
    Overlapping variant regions from other studies: 130 SVs from 29 studies. See in: genome view    
    Submitted genomic83,722,258-83,722,258Question Mark
    Overlapping variant regions from other studies: 130 SVs from 29 studies. See in: genome view    
    Submitted genomic83,722,258-83,722,258Question Mark
    Overlapping variant regions from other studies: 134 SVs from 29 studies. See in: genome view    
    Submitted genomic84,200,261-84,200,261Question Mark
    Overlapping variant regions from other studies: 134 SVs from 29 studies. See in: genome view    
    Submitted genomic84,200,262-84,200,262Question Mark
    Overlapping variant regions from other studies: 135 SVs from 33 studies. See in: genome view    
    Submitted genomic84,338,529-84,338,529Question Mark
    Overlapping variant regions from other studies: 135 SVs from 33 studies. See in: genome view    
    Submitted genomic84,338,531-84,338,531Question Mark
    Overlapping variant regions from other studies: 140 SVs from 30 studies. See in: genome view    
    Submitted genomic84,510,509-84,510,509Question Mark
    Overlapping variant regions from other studies: 140 SVs from 30 studies. See in: genome view    
    Submitted genomic84,510,511-84,510,511Question Mark
    Overlapping variant regions from other studies: 122 SVs from 27 studies. See in: genome view    
    Submitted genomic84,906,938-84,906,938Question Mark
    Overlapping variant regions from other studies: 122 SVs from 27 studies. See in: genome view    
    Submitted genomic84,906,953-84,906,953Question Mark
    Overlapping variant regions from other studies: 101 SVs from 22 studies. See in: genome view    
    Submitted genomic85,077,794-85,077,794Question Mark
    Overlapping variant regions from other studies: 101 SVs from 22 studies. See in: genome view    
    Submitted genomic85,077,800-85,077,800Question Mark
    Overlapping variant regions from other studies: 126 SVs from 28 studies. See in: genome view    
    Submitted genomic85,197,029-85,197,029Question Mark
    Overlapping variant regions from other studies: 126 SVs from 28 studies. See in: genome view    
    Submitted genomic85,197,052-85,197,052Question Mark
    Overlapping variant regions from other studies: 126 SVs from 28 studies. See in: genome view    
    Submitted genomic85,197,066-85,197,066Question Mark
    Overlapping variant regions from other studies: 126 SVs from 28 studies. See in: genome view    
    Submitted genomic85,197,067-85,197,067Question Mark
    Overlapping variant regions from other studies: 95 SVs from 24 studies. See in: genome view    
    Submitted genomic85,888,156-85,888,156Question Mark
    Overlapping variant regions from other studies: 95 SVs from 24 studies. See in: genome view    
    Submitted genomic85,888,158-85,888,158Question Mark
    Overlapping variant regions from other studies: 97 SVs from 22 studies. See in: genome view    
    Submitted genomic85,934,408-85,934,408Question Mark
    Overlapping variant regions from other studies: 97 SVs from 22 studies. See in: genome view    
    Submitted genomic85,934,411-85,934,411Question Mark
    Overlapping variant regions from other studies: 102 SVs from 24 studies. See in: genome view    
    Submitted genomic85,982,977-85,982,977Question Mark
    Overlapping variant regions from other studies: 102 SVs from 24 studies. See in: genome view    
    Submitted genomic85,982,977-85,982,977Question Mark
    Overlapping variant regions from other studies: 87 SVs from 19 studies. See in: genome view    
    Submitted genomic86,217,685-86,217,685Question Mark
    Overlapping variant regions from other studies: 87 SVs from 19 studies. See in: genome view    
    Submitted genomic86,217,685-86,217,685Question Mark
    Overlapping variant regions from other studies: 88 SVs from 22 studies. See in: genome view    
    Submitted genomic86,497,608-86,497,608Question Mark
    Overlapping variant regions from other studies: 88 SVs from 22 studies. See in: genome view    
    Submitted genomic86,497,616-86,497,616Question Mark
    Overlapping variant regions from other studies: 173 SVs from 26 studies. See in: genome view    
    Submitted genomic109,534,981-109,534,981Question Mark
    Overlapping variant regions from other studies: 173 SVs from 26 studies. See in: genome view    
    Submitted genomic109,534,991-109,534,991Question Mark
    Overlapping variant regions from other studies: 173 SVs from 26 studies. See in: genome view    
    Submitted genomic109,535,232-109,535,232Question Mark
    Overlapping variant regions from other studies: 173 SVs from 26 studies. See in: genome view    
    Submitted genomic109,535,249-109,535,249Question Mark
    Overlapping variant regions from other studies: 162 SVs from 21 studies. See in: genome view    
    Submitted genomic83,976,363-83,976,363Question Mark
    Overlapping variant regions from other studies: 162 SVs from 21 studies. See in: genome view    
    Submitted genomic83,977,014-83,977,014Question Mark
    Overlapping variant regions from other studies: 168 SVs from 20 studies. See in: genome view    
    Submitted genomic84,536,963-84,536,963Question Mark
    Overlapping variant regions from other studies: 168 SVs from 20 studies. See in: genome view    
    Submitted genomic84,536,965-84,536,965Question Mark
    Overlapping variant regions from other studies: 160 SVs from 19 studies. See in: genome view    
    Submitted genomic84,564,825-84,564,825Question Mark
    Overlapping variant regions from other studies: 160 SVs from 19 studies. See in: genome view    
    Submitted genomic84,564,830-84,564,830Question Mark
    Overlapping variant regions from other studies: 157 SVs from 21 studies. See in: genome view    
    Submitted genomic84,729,713-84,729,713Question Mark
    Overlapping variant regions from other studies: 157 SVs from 21 studies. See in: genome view    
    Submitted genomic84,729,717-84,729,717Question Mark
    Overlapping variant regions from other studies: 157 SVs from 21 studies. See in: genome view    
    Submitted genomic84,739,332-84,739,332Question Mark
    Overlapping variant regions from other studies: 157 SVs from 21 studies. See in: genome view    
    Submitted genomic84,739,332-84,739,332Question Mark
    Overlapping variant regions from other studies: 155 SVs from 23 studies. See in: genome view    
    Submitted genomic84,789,346-84,789,346Question Mark
    Overlapping variant regions from other studies: 155 SVs from 23 studies. See in: genome view    
    Submitted genomic84,789,346-84,789,346Question Mark
    Overlapping variant regions from other studies: 88 SVs from 14 studies. See in: genome view    
    Submitted genomic19,020,444-19,020,444Question Mark
    Overlapping variant regions from other studies: 88 SVs from 14 studies. See in: genome view    
    Submitted genomic19,020,446-19,020,446Question Mark
    Overlapping variant regions from other studies: 131 SVs from 20 studies. See in: genome view    
    Submitted genomic36,549,057-36,549,057Question Mark
    Overlapping variant regions from other studies: 131 SVs from 20 studies. See in: genome view    
    Submitted genomic36,549,057-36,549,057Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3105,488,273105,488,273-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3105,488,274105,488,274+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3105,962,240105,962,240+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3105,962,240105,962,240-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3106,108,623106,108,623+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3106,108,624106,108,624-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3106,830,619106,830,619+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3106,830,620106,830,620-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3107,706,152107,706,152+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3107,706,155107,706,155-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3108,651,910108,651,910+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3108,651,916108,651,916-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3109,096,778109,096,778+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3109,097,268109,097,268-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3120,208,269120,208,269+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3120,208,275120,208,275-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3154,775,336154,775,336+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3154,775,345154,775,345-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3154,833,957154,833,957+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3154,833,959154,833,959-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3154,836,803154,836,803+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3154,836,815154,836,815-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3155,027,218155,027,218-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3155,027,227155,027,227+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3156,107,069156,107,069+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3156,107,070156,107,070-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr383,070,80483,070,804+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr383,070,80683,070,806-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr383,098,72683,098,726+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr383,098,79483,098,794-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr383,098,94683,098,946-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr383,098,95583,098,955+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr383,126,41783,126,417+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr383,126,42083,126,420-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr383,673,10783,673,107+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr383,673,10783,673,107-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr384,151,11084,151,110+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr384,151,11184,151,111-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr384,289,37884,289,378-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr384,289,38084,289,380+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr384,461,35884,461,358-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr384,461,36084,461,360+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr384,857,78784,857,787+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr384,857,80284,857,802-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr385,028,64385,028,643+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr385,028,64985,028,649-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr385,147,87985,147,879-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr385,147,90285,147,902+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr385,147,91685,147,916+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr385,147,91785,147,917-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr385,839,00685,839,006+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr385,839,00885,839,008-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr385,885,25885,885,258-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr385,885,26185,885,261+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr385,933,82785,933,827+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr385,933,82785,933,827-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr386,168,53586,168,535+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr386,168,53586,168,535-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr386,448,45886,448,458+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr386,448,46686,448,466-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8108,522,752108,522,752-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8108,522,762108,522,762+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8108,523,003108,523,003+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr8108,523,020108,523,020-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr883,064,12883,064,128+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr883,064,77983,064,779-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr883,624,72883,624,728+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr883,624,73083,624,730-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr883,652,59083,652,590+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr883,652,59583,652,595-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr883,817,47883,817,478-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr883,817,48283,817,482+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr883,827,09783,827,097+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr883,827,09783,827,097-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr883,877,11183,877,111+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr883,877,11183,877,111-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr2019,039,80019,039,800+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr2019,039,80219,039,802-
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr2037,920,65537,920,655+
    nsv7098706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr2037,920,65537,920,655-
    nsv7098706RemappedPerfectGRCh38.p12PATCHESSecond PassNW_018654711.1Chr3|NW_01
    8654711.1    		57,82057,820+
    nsv7098706RemappedPerfectGRCh38.p12PATCHESSecond PassNW_018654711.1Chr3|NW_01
    8654711.1    		57,83557,835-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3105,207,117105,207,117-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3105,207,118105,207,118+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3105,681,087105,681,087+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3105,681,087105,681,087-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3105,827,470105,827,470+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3105,827,471105,827,471-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3106,549,466106,549,466+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3106,549,467106,549,467-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3107,424,999107,424,999+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3107,425,002107,425,002-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3108,370,757108,370,757+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3108,370,763108,370,763-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3108,815,625108,815,625+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3108,816,115108,816,115-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3119,927,116119,927,116+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3119,927,122119,927,122-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3154,493,125154,493,125+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3154,493,134154,493,134-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3154,551,746154,551,746+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3154,551,748154,551,748-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3154,554,592154,554,592+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3154,554,604154,554,604-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3154,745,007154,745,007-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3154,745,016154,745,016+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3155,824,858155,824,858+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3155,824,859155,824,859-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr383,119,95583,119,955+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr383,119,95783,119,957-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr383,147,87783,147,877+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr383,147,94583,147,945-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr383,148,09783,148,097-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr383,148,10683,148,106+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr383,175,56883,175,568+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr383,175,57183,175,571-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr383,722,25883,722,258+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr383,722,25883,722,258-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr384,200,26184,200,261+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr384,200,26284,200,262-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr384,338,52984,338,529-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr384,338,53184,338,531+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr384,510,50984,510,509-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr384,510,51184,510,511+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr384,906,93884,906,938+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr384,906,95384,906,953-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr385,077,79485,077,794+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr385,077,80085,077,800-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr385,197,02985,197,029-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr385,197,05285,197,052+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr385,197,06685,197,066+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr385,197,06785,197,067-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr385,888,15685,888,156+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr385,888,15885,888,158-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr385,934,40885,934,408-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr385,934,41185,934,411+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr385,982,97785,982,977+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr385,982,97785,982,977-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr386,217,68586,217,685+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr386,217,68586,217,685-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr386,497,60886,497,608+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr386,497,61686,497,616-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8109,534,981109,534,981-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8109,534,991109,534,991+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8109,535,232109,535,232+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr8109,535,249109,535,249-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr883,976,36383,976,363+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr883,977,01483,977,014-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr884,536,96384,536,963+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr884,536,96584,536,965-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr884,564,82584,564,825+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr884,564,83084,564,830-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr884,729,71384,729,713-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr884,729,71784,729,717+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr884,739,33284,739,332+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr884,739,33284,739,332-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr884,789,34684,789,346+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000008.10Chr884,789,34684,789,346-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000020.10Chr2019,020,44419,020,444+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000020.10Chr2019,020,44619,020,446-
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000020.10Chr2036,549,05736,549,057+
    nsv7098706Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000020.10Chr2036,549,05736,549,057-

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv18792403intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792389intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792385intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792386intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792387intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792433intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792426interchromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792432interchromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792427intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792404intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792405intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792407intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792406intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792408intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792402intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792390intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792388intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792410intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792411intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792409intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792414interchromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792401intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792413interchromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792419intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792420interchromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792423intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792422intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792425interchromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792424intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792421interchromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792416interchromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792415interchromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792418interchromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792428interchromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792412interchromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792434interchromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792430interchromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792417intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792429intrachromosomal translocationFHU15-170SequencingSequence alignment40
    nssv18792431interchromosomal translocationFHU15-170SequencingSequence alignment40

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
    nssv18792403RemappedPerfectGRCh38.p12Second PassNW_018654711.1Chr3|NW_01
    8654711.1    		57,82057,820+
    nssv18792389RemappedPerfectGRCh38.p12Second PassNW_018654711.1Chr3|NW_01
    8654711.1    		57,83557,835-
    nssv18792385RemappedPerfectGRCh38.p12First PassNC_000003.12Chr383,070,80483,070,804+
    nssv18792386RemappedPerfectGRCh38.p12First PassNC_000003.12Chr383,070,80683,070,806-
    nssv18792387RemappedPerfectGRCh38.p12First PassNC_000003.12Chr383,098,72683,098,726+
    nssv18792433RemappedPerfectGRCh38.p12First PassNC_000003.12Chr383,098,79483,098,794-
    nssv18792426RemappedPerfectGRCh38.p12First PassNC_000003.12Chr383,098,94683,098,946-
    nssv18792432RemappedPerfectGRCh38.p12First PassNC_000003.12Chr383,098,95583,098,955+
    nssv18792427RemappedPerfectGRCh38.p12First PassNC_000003.12Chr383,126,41783,126,417+
    nssv18792404RemappedPerfectGRCh38.p12First PassNC_000003.12Chr383,126,42083,126,420-
    nssv18792386RemappedPerfectGRCh38.p12First PassNC_000003.12Chr383,673,10783,673,107-
    nssv18792405RemappedPerfectGRCh38.p12First PassNC_000003.12Chr383,673,10783,673,107+
    nssv18792385RemappedPerfectGRCh38.p12First PassNC_000003.12Chr384,151,11084,151,110+
    nssv18792407RemappedPerfectGRCh38.p12First PassNC_000003.12Chr384,151,11184,151,111-
    nssv18792406RemappedPerfectGRCh38.p12First PassNC_000003.12Chr384,289,37884,289,378-
    nssv18792408RemappedPerfectGRCh38.p12First PassNC_000003.12Chr384,289,38084,289,380+
    nssv18792402RemappedPerfectGRCh38.p12First PassNC_000003.12Chr384,461,35884,461,358-
    nssv18792405RemappedPerfectGRCh38.p12First PassNC_000003.12Chr384,461,36084,461,360+
    nssv18792403RemappedPerfectGRCh38.p12First PassNC_000003.12Chr384,857,78784,857,787+
    nssv18792389RemappedPerfectGRCh38.p12First PassNC_000003.12Chr384,857,80284,857,802-
    nssv18792390RemappedPerfectGRCh38.p12First PassNC_000003.12Chr385,028,64385,028,643+
    nssv18792389RemappedPerfectGRCh38.p12First PassNC_000003.12Chr385,028,64985,028,649-
    nssv18792387RemappedPerfectGRCh38.p12First PassNC_000003.12Chr385,147,87985,147,879-
    nssv18792388RemappedPerfectGRCh38.p12First PassNC_000003.12Chr385,147,90285,147,902+
    nssv18792388RemappedPerfectGRCh38.p12First PassNC_000003.12Chr385,147,91685,147,916+
    nssv18792406RemappedPerfectGRCh38.p12First PassNC_000003.12Chr385,147,91785,147,917-
    nssv18792407RemappedPerfectGRCh38.p12First PassNC_000003.12Chr385,839,00685,839,006+
    nssv18792410RemappedPerfectGRCh38.p12First PassNC_000003.12Chr385,839,00885,839,008-
    nssv18792410RemappedPerfectGRCh38.p12First PassNC_000003.12Chr385,885,25885,885,258-
    nssv18792411RemappedPerfectGRCh38.p12First PassNC_000003.12Chr385,885,26185,885,261+
    nssv18792404RemappedPerfectGRCh38.p12First PassNC_000003.12Chr385,933,82785,933,827-
    nssv18792409RemappedPerfectGRCh38.p12First PassNC_000003.12Chr385,933,82785,933,827+
    nssv18792403RemappedPerfectGRCh38.p12First PassNC_000003.12Chr386,168,53586,168,535+
    nssv18792408RemappedPerfectGRCh38.p12First PassNC_000003.12Chr386,168,53586,168,535-
    nssv18792409RemappedPerfectGRCh38.p12First PassNC_000003.12Chr386,448,45886,448,458+
    nssv18792414RemappedPerfectGRCh38.p12First PassNC_000003.12Chr386,448,46686,448,466-
    nssv18792401RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3105,488,273105,488,273-
    nssv18792413RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3105,488,274105,488,274+
    nssv18792390RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3105,962,240105,962,240+
    nssv18792419RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3105,962,240105,962,240-
    nssv18792420RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3106,108,623106,108,623+
    nssv18792423RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3106,108,624106,108,624-
    nssv18792422RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3106,830,619106,830,619+
    nssv18792425RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3106,830,620106,830,620-
    nssv18792424RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3107,706,152107,706,152+
    nssv18792421RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3107,706,155107,706,155-
    nssv18792422RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3108,651,910108,651,910+
    nssv18792416RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3108,651,916108,651,916-
    nssv18792415RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3109,096,778109,096,778+
    nssv18792418RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3109,097,268109,097,268-
    nssv18792419RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3120,208,269120,208,269+
    nssv18792402RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3120,208,275120,208,275-
    nssv18792401RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3154,775,336154,775,336+
    nssv18792424RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3154,775,345154,775,345-
    nssv18792423RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3154,833,957154,833,957+
    nssv18792427RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3154,833,959154,833,959-
    nssv18792428RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3154,836,803154,836,803+
    nssv18792433RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3154,836,815154,836,815-
    nssv18792412RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3155,027,218155,027,218-
    nssv18792434RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3155,027,227155,027,227+
    nssv18792411RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3156,107,069156,107,069+
    nssv18792430RemappedPerfectGRCh38.p12First PassNC_000003.12Chr3156,107,070156,107,070-
    nssv18792415RemappedPerfectGRCh38.p12First PassNC_000008.11Chr883,064,12883,064,128+
    nssv18792417RemappedPerfectGRCh38.p12First PassNC_000008.11Chr883,064,77983,064,779-
    nssv18792418RemappedPerfectGRCh38.p12First PassNC_000008.11Chr883,624,72883,624,728+
    nssv18792416RemappedPerfectGRCh38.p12First PassNC_000008.11Chr883,624,73083,624,730-
    nssv18792417RemappedPerfectGRCh38.p12First PassNC_000008.11Chr883,652,59083,652,590+
    nssv18792429RemappedPerfectGRCh38.p12First PassNC_000008.11Chr883,652,59583,652,595-
    nssv18792421RemappedPerfectGRCh38.p12First PassNC_000008.11Chr883,817,47883,817,478-
    nssv18792428RemappedPerfectGRCh38.p12First PassNC_000008.11Chr883,817,48283,817,482+
    nssv18792412RemappedPerfectGRCh38.p12First PassNC_000008.11Chr883,827,09783,827,097-
    nssv18792420RemappedPerfectGRCh38.p12First PassNC_000008.11Chr883,827,09783,827,097+
    nssv18792413RemappedPerfectGRCh38.p12First PassNC_000008.11Chr883,877,11183,877,111+
    nssv18792431RemappedPerfectGRCh38.p12First PassNC_000008.11Chr883,877,11183,877,111-
    nssv18792426RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8108,522,752108,522,752-
    nssv18792432RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8108,522,762108,522,762+
    nssv18792425RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8108,523,003108,523,003+
    nssv18792429RemappedPerfectGRCh38.p12First PassNC_000008.11Chr8108,523,020108,523,020-
    nssv18792414RemappedPerfectGRCh38.p12First PassNC_000020.11Chr2019,039,80019,039,800+
    nssv18792430RemappedPerfectGRCh38.p12First PassNC_000020.11Chr2019,039,80219,039,802-
    nssv18792431RemappedPerfectGRCh38.p12First PassNC_000020.11Chr2037,920,65537,920,655+
    nssv18792434RemappedPerfectGRCh38.p12First PassNC_000020.11Chr2037,920,65537,920,655-
    nssv18792385Submitted genomicGRCh37 (hg19)NC_000003.11Chr383,119,95583,119,955+
    nssv18792386Submitted genomicGRCh37 (hg19)NC_000003.11Chr383,119,95783,119,957-
    nssv18792387Submitted genomicGRCh37 (hg19)NC_000003.11Chr383,147,87783,147,877+
    nssv18792433Submitted genomicGRCh37 (hg19)NC_000003.11Chr383,147,94583,147,945-
    nssv18792426Submitted genomicGRCh37 (hg19)NC_000003.11Chr383,148,09783,148,097-
    nssv18792432Submitted genomicGRCh37 (hg19)NC_000003.11Chr383,148,10683,148,106+
    nssv18792427Submitted genomicGRCh37 (hg19)NC_000003.11Chr383,175,56883,175,568+
    nssv18792404Submitted genomicGRCh37 (hg19)NC_000003.11Chr383,175,57183,175,571-
    nssv18792386Submitted genomicGRCh37 (hg19)NC_000003.11Chr383,722,25883,722,258-
    nssv18792405Submitted genomicGRCh37 (hg19)NC_000003.11Chr383,722,25883,722,258+
    nssv18792385Submitted genomicGRCh37 (hg19)NC_000003.11Chr384,200,26184,200,261+
    nssv18792407Submitted genomicGRCh37 (hg19)NC_000003.11Chr384,200,26284,200,262-
    nssv18792406Submitted genomicGRCh37 (hg19)NC_000003.11Chr384,338,52984,338,529-
    nssv18792408Submitted genomicGRCh37 (hg19)NC_000003.11Chr384,338,53184,338,531+
    nssv18792402Submitted genomicGRCh37 (hg19)NC_000003.11Chr384,510,50984,510,509-
    nssv18792405Submitted genomicGRCh37 (hg19)NC_000003.11Chr384,510,51184,510,511+
    nssv18792403Submitted genomicGRCh37 (hg19)NC_000003.11Chr384,906,93884,906,938+
    nssv18792389Submitted genomicGRCh37 (hg19)NC_000003.11Chr384,906,95384,906,953-
    Showing 100 of 162

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    No genotype data were submitted for this variant

    You are here: NCBI
    Support Center