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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6314523complex chromosomal rearrangement3nstd102humanPathogenic GRCh37 chr5: 119,485,964-119,485,964 , GRCh37 chr5: 119,486,003-119,486,003 , GRCh37 chr5: 119,486,172-119,486,172 , GRCh37 chr5: 119,486,176-119,486,176 , GRCh38.p12 chr5: 120,150,269-120,150,269 , GRCh38.p12 chr5: 120,150,308-120,150,308 , GRCh38.p12 chr5: 120,150,477-120,150,477 , GRCh38.p12 chr5: 120,150,481-120,150,481 , GRCh38.p12 chr2: 148,258,393-148,258,393 , GRCh38.p12 chr2: 148,259,189-148,259,189 , GRCh37 chr2: 149,016,758-149,016,758 , GRCh37 chr2: 149,015,962-149,015,962 MBD5
    nsv6314503complex chromosomal rearrangement3nstd102humanUncertain significance GRCh37 chrX: 154,390,041-154,390,041 , GRCh37 chrX: 655,153-655,153 , GRCh37 chrX: 698,657-698,657 , GRCh37 chrX: 135,300,376-135,300,376 , GRCh37 chrX: 135,300,477-135,300,477 , GRCh37 chrX: 154,385,238-154,385,238 , GRCh38.p12 chrX: 694,418-694,418 , GRCh38.p12 chrX: 737,922-737,922 , GRCh38.p12 chrX: 136,218,217-136,218,217 , GRCh38.p12 chrX: 136,218,318-136,218,318 , GRCh38.p12 chrX: 155,156,963-155,156,963 , GRCh38.p12 chrX: 155,161,766-155,161,766 MAP7D3
    nsv6314485complex chromosomal rearrangement3nstd102humanUncertain significance GRCh37 chrX: 154,390,213-154,390,213 , GRCh37 chrX: 655,195-655,195 , GRCh37 chrX: 698,367-698,367 , GRCh37 chrX: 135,300,329-135,300,329 , GRCh37 chrX: 135,300,418-135,300,418 , GRCh37 chrX: 154,388,192-154,388,192 , GRCh38.p12 chrX: 694,460-694,460 , GRCh38.p12 chrX: 737,632-737,632 , GRCh38.p12 chrX: 136,218,170-136,218,170 , GRCh38.p12 chrX: 136,218,259-136,218,259 , GRCh38.p12 chrX: 155,159,917-155,159,917 , GRCh38.p12 chrX: 155,161,938-155,161,938 MAP7D3
    nsv6314228complex chromosomal rearrangement4nstd102humanUncertain significance GRCh37 chr17: 68,765,841-68,765,841 , GRCh37 chr17: 68,765,842-68,765,842 , GRCh37 chr17: 69,040,502-69,040,502 , GRCh37 chr17: 69,040,503-69,040,503 , GRCh38.p12 chr17: 70,769,701-70,769,701 , GRCh38.p12 chr17: 71,044,362-71,044,362 , GRCh38.p12 chr17: 71,044,361-71,044,361 , GRCh38.p12 chr17: 70,769,700-70,769,700 , GRCh37 chr7: 10,805,063-10,805,063 , GRCh37 chr7: 10,805,065-10,805,065 , GRCh38.p12 chr7: 10,765,436-10,765,436 , GRCh38.p12 chr7: 10,765,438-10,765,438 , GRCh38.p12 chr6: 16,030,475-16,030,475 , GRCh38.p12 chr6: 16,030,478-16,030,478 , GRCh37 chr6: 16,030,706-16,030,706 , GRCh37 chr6: 16,030,709-16,030,709 MGC4859
    nsv6314478complex chromosomal rearrangement3nstd102humanPathogenic GRCh38.p12 chr13: 101,317,547-101,317,547 , GRCh38.p12 chr13: 101,321,256-101,321,256 , GRCh38.p12 chr13: 108,561,681-108,561,681 , GRCh38.p12 chr13: 108,561,710-108,561,710 , GRCh37 chr13: 109,214,029-109,214,029 , GRCh37 chr13: 109,214,058-109,214,058 , GRCh37 chr13: 101,969,898-101,969,898 , GRCh37 chr13: 101,973,607-101,973,607 , GRCh37 chr7: 49,277,729-49,277,729 , GRCh37 chr7: 49,277,887-49,277,887 , GRCh38.p12 chr7: 49,238,133-49,238,133 , GRCh38.p12 chr7: 49,238,291-49,238,291 MYO16, NALCN
    nsv6314469complex chromosomal rearrangement3nstd102humanPathogenic GRCh38.p12 chr2: 224,530,224-224,530,224 , GRCh38.p12 chr2: 224,530,225-224,530,225 , GRCh38.p12 chr2: 224,916,514-224,916,514 , GRCh38.p12 chr2: 224,920,190-224,920,190 , GRCh37 chr2: 225,781,231-225,781,231 , GRCh37 chr2: 225,784,907-225,784,907 , GRCh37 chr2: 225,394,941-225,394,941 , GRCh37 chr2: 225,394,942-225,394,942 , GRCh38.p12 chr1: 20,558,564-20,558,564 , GRCh38.p12 chr1: 20,558,570-20,558,570 , GRCh37 chr1: 20,885,057-20,885,057 , GRCh37 chr1: 20,885,063-20,885,063 CUL3, DOCK10
    nsv6314402complex chromosomal rearrangement4nstd102humanPathogenic GRCh38.p12 chr16: 63,881,919-63,881,919 , GRCh38.p12 chr16: 63,881,920-63,881,920 , GRCh37 chr16: 63,915,823-63,915,823 , GRCh37 chr16: 63,915,824-63,915,824 , GRCh38.p12 chr2: 48,489,716-48,489,716 , GRCh38.p12 chr2: 48,489,724-48,489,724 , GRCh38.p12 chr2: 50,918,204-50,918,204 , GRCh38.p12 chr2: 59,862,802-59,862,802 , GRCh38.p12 chr2: 59,862,801-59,862,801 , GRCh38.p12 chr2: 50,918,205-50,918,205 , GRCh37 chr2: 48,716,855-48,716,855 , GRCh37 chr2: 48,716,863-48,716,863 , GRCh37 chr2: 51,145,342-51,145,342 , GRCh37 chr2: 51,145,343-51,145,343 , GRCh37 chr2: 60,089,936-60,089,936 , GRCh37 chr2: 60,089,937-60,089,937 NRXN1, PPP1R21
    nsv6314630complex chromosomal rearrangement3nstd102humanLikely pathogenic GRCh37 chr20: 55,982,643-55,982,643 , GRCh37 chr20: 55,982,746-55,982,746 , GRCh37 chr20: 55,982,746-55,982,746 , GRCh37 chr20: 55,984,328-55,984,328 , GRCh38.p12 chr20: 57,407,587-57,407,587 , GRCh38.p12 chr20: 57,407,690-57,407,690 , GRCh38.p12 chr20: 57,407,690-57,407,690 , GRCh38.p12 chr20: 57,409,272-57,409,272 , GRCh37 chr11: 73,839,840-73,839,840 , GRCh37 chr11: 73,841,465-73,841,465 , GRCh38.p12 chr11: 74,128,795-74,128,795 , GRCh38.p12 chr11: 74,130,420-74,130,420 C2CD3, RBM38
    nsv6314539complex chromosomal rearrangement5nstd102humanLikely pathogenic GRCh37 chr11: 1,915,057-1,915,057 , GRCh37 chr11: 1,915,843-1,915,843 , GRCh37 chr11: 1,936,668-1,936,668 , GRCh37 chr11: 1,936,993-1,936,993 , GRCh37 chr11: 1,960,727-1,960,727 , GRCh37 chr11: 1,961,361-1,961,361 , GRCh37 chr11: 1,984,895-1,984,895 , GRCh37 chr11: 1,985,019-1,985,019 , GRCh38.p12 chr11: 1,893,827-1,893,827 , GRCh38.p12 chr11: 1,894,613-1,894,613 , GRCh38.p12 chr11: 1,963,665-1,963,665 , GRCh38.p12 chr11: 1,963,789-1,963,789 , GRCh38.p12 chr11: 1,915,438-1,915,438 , GRCh38.p12 chr11: 1,915,763-1,915,763 , GRCh38.p12 chr11: 1,939,497-1,939,497 , GRCh38.p12 chr11: 1,940,131-1,940,131 , GRCh38.p12 chr2: 69,361,132-69,361,132 , GRCh38.p12 chr2: 69,361,288-69,361,288 , GRCh37 chr2: 69,588,264-69,588,264 , GRCh37 chr2: 69,588,420-69,588,420 GFPT1, MRPL23
    nsv6314464complex chromosomal rearrangement3nstd102humanLikely pathogenic GRCh38.p12 chr14: 33,542,762-33,542,762 , GRCh38.p12 chr14: 33,542,762-33,542,762 , GRCh38.p12 chr14: 31,095,459-31,095,459 , GRCh38.p12 chr14: 31,095,460-31,095,460 , GRCh37 chr14: 34,011,968-34,011,968 , GRCh37 chr14: 34,011,968-34,011,968 , GRCh37 chr14: 31,564,665-31,564,665 , GRCh37 chr14: 31,564,666-31,564,666 , GRCh38.p12 chr4: 22,580,380-22,580,380 , GRCh38.p12 chr4: 22,580,380-22,580,380 , GRCh37 chr4: 22,582,003-22,582,003 , GRCh37 chr4: 22,582,003-22,582,003 AP4S1, NPAS3
    nsv6314406complex chromosomal rearrangement4nstd102humanLikely pathogenic GRCh38.p12 chr14: 70,739,456-70,739,456 , GRCh38.p12 chr14: 70,739,498-70,739,498 , GRCh38.p12 chr14: 78,670,191-78,670,191 , GRCh38.p12 chr14: 78,670,195-78,670,195 , GRCh38.p12 chr14: 81,624,408-81,624,408 , GRCh38.p12 chr14: 81,624,552-81,624,552 , GRCh37 chr14: 71,206,173-71,206,173 , GRCh37 chr14: 71,206,215-71,206,215 , GRCh37 chr14: 79,136,534-79,136,534 , GRCh37 chr14: 79,136,538-79,136,538 , GRCh37 chr14: 82,090,752-82,090,752 , GRCh37 chr14: 82,090,896-82,090,896 , GRCh38.p12 chr2: 38,118,356-38,118,356 , GRCh38.p12 chr2: 38,118,359-38,118,359 , GRCh37 chr2: 38,345,498-38,345,498 , GRCh37 chr2: 38,345,501-38,345,501 MAP3K9, NRXN3
    nsv6314508complex chromosomal rearrangement3nstd102humanUncertain significance GRCh38.p12 chr9: 77,426,009-77,426,009 , GRCh38.p12 chr9: 77,426,009-77,426,009 , GRCh37 chr9: 80,040,925-80,040,925 , GRCh37 chr9: 80,040,925-80,040,925 , GRCh38.p12 chr6: 97,322,974-97,322,974 , GRCh38.p12 chr6: 97,322,985-97,322,985 , GRCh38.p12 chr6: 97,500,336-97,500,336 , GRCh38.p12 chr6: 97,500,337-97,500,337 , GRCh37 chr6: 97,770,850-97,770,850 , GRCh37 chr6: 97,770,861-97,770,861 , GRCh37 chr6: 97,948,212-97,948,212 , GRCh37 chr6: 97,948,213-97,948,213 GNA14, LOC101927314
    nsv6314421complex chromosomal rearrangement3nstd102humanUncertain significance GRCh38.p12 chr22: 31,226,472-31,226,472 , GRCh38.p12 chr22: 31,226,484-31,226,484 , GRCh38.p12 chr22: 31,226,484-31,226,484 , GRCh38.p12 chr22: 31,226,615-31,226,615 , GRCh37 chr22: 31,622,458-31,622,458 , GRCh37 chr22: 31,622,470-31,622,470 , GRCh37 chr22: 31,622,470-31,622,470 , GRCh37 chr22: 31,622,601-31,622,601 , GRCh37 chrX: 62,683,198-62,683,198 , GRCh37 chrX: 62,683,200-62,683,200 , GRCh38.p12 chrX: 63,463,318-63,463,318 , GRCh38.p12 chrX: 63,463,320-63,463,320 LIMK2, LINC01278
    nsv6314386complex chromosomal rearrangement5nstd102humanUncertain significance GRCh38.p12 chr16: 55,052,894-55,052,894 , GRCh38.p12 chr16: 55,052,894-55,052,894 , GRCh37 chr16: 55,086,806-55,086,806 , GRCh37 chr16: 55,086,806-55,086,806 , GRCh38.p12 chr10: 84,763,363-84,763,363 , GRCh38.p12 chr10: 48,925,282-48,925,282 , GRCh38.p12 chr10: 48,925,288-48,925,288 , GRCh38.p12 chr10: 84,762,420-84,762,420 , GRCh37 chr10: 86,523,119-86,523,119 , GRCh37 chr10: 50,133,327-50,133,327 , GRCh37 chr10: 50,133,333-50,133,333 , GRCh37 chr10: 86,522,176-86,522,176 , GRCh38.p12 chr9: 102,842,491-102,842,491 , GRCh38.p12 chr9: 102,842,491-102,842,491 , GRCh37 chr9: 105,604,773-105,604,773 , GRCh37 chr9: 105,604,773-105,604,773 , GRCh37 chr7: 118,838,492-118,838,492 , GRCh37 chr7: 118,838,590-118,838,590 , GRCh38.p12 chr7: 119,198,438-119,198,438 , GRCh38.p12 chr7: 119,198,536-119,198,536 WDFY4, LRRC18
    nsv6314357complex chromosomal rearrangement12nstd102humanUncertain significance GRCh38.p12 chr10: 54,033,420-54,033,420 , GRCh38.p12 chr10: 54,033,422-54,033,422 , GRCh38.p12 chr10: 55,760,153-55,760,153 , GRCh38.p12 chr10: 55,760,153-55,760,153 , GRCh38.p12 chr10: 55,760,157-55,760,157 , GRCh38.p12 chr10: 55,761,328-55,761,328 , GRCh38.p12 chr10: 55,761,340-55,761,340 , GRCh38.p12 chr10: 55,764,027-55,764,027 , GRCh38.p12 chr10: 55,764,045-55,764,045 , GRCh37 chr10: 55,793,180-55,793,180 , GRCh37 chr10: 55,793,182-55,793,182 , GRCh37 chr10: 57,519,913-57,519,913 , GRCh37 chr10: 57,519,913-57,519,913 , GRCh37 chr10: 57,519,917-57,519,917 , GRCh37 chr10: 57,521,088-57,521,088 , GRCh37 chr10: 57,521,100-57,521,100 , GRCh37 chr10: 57,523,787-57,523,787 , GRCh37 chr10: 57,523,805-57,523,805 , GRCh38.p12 chr4: 101,366,634-101,366,634 , GRCh38.p12 chr4: 101,366,641-101,366,641 , GRCh38.p12 chr4: 104,113,993-104,113,993 , GRCh38.p12 chr4: 104,115,551-104,115,551 , GRCh38.p12 chr4: 104,115,578-104,115,578 , GRCh38.p12 chr4: 104,824,626-104,824,626 , GRCh38.p12 chr4: 104,824,671-104,824,671 , GRCh38.p12 chr4: 103,816,979-103,816,979 , GRCh38.p12 chr4: 103,817,839-103,817,839 , GRCh38.p12 chr4: 104,104,543-104,104,543 , GRCh38.p12 chr4: 104,107,238-104,107,238 , GRCh38.p12 chr4: 104,107,243-104,107,243 , GRCh38.p12 chr4: 104,108,613-104,108,613 , GRCh37 chr4: 102,287,791-102,287,791 , GRCh37 chr4: 102,287,798-102,287,798 , GRCh37 chr4: 105,035,150-105,035,150 , GRCh37 chr4: 105,036,708-105,036,708 , GRCh37 chr4: 105,036,735-105,036,735 , GRCh37 chr4: 105,745,783-105,745,783 , GRCh37 chr4: 105,745,828-105,745,828 , GRCh37 chr4: 104,738,136-104,738,136 , GRCh37 chr4: 104,738,996-104,738,996 , GRCh37 chr4: 105,025,700-105,025,700 , GRCh37 chr4: 105,028,395-105,028,395 , GRCh37 chr4: 105,028,400-105,028,400 , GRCh37 chr4: 105,029,770-105,029,770 , GRCh38.p12 chr1: 50,295,791-50,295,791 , GRCh38.p12 chr1: 50,295,798-50,295,798 , GRCh37 chr1: 50,761,463-50,761,463 , GRCh37 chr1: 50,761,470-50,761,470 PCDH15, LINC02808
    nsv6314261complex chromosomal rearrangement2nstd102humanUncertain significance GRCh38.p12 chr4: 174,079,140-174,079,140 , GRCh38.p12 chr4: 184,176,792-184,176,792 , GRCh38.p12 chr4: 188,901,617-188,901,617 , GRCh38.p12 chr4: 188,920,643-188,920,643 , GRCh37 chr4: 175,000,291-175,000,291 , GRCh37 chr4: 185,097,945-185,097,945 , GRCh37 chr4: 189,822,771-189,822,771 , GRCh37 chr4: 189,841,797-189,841,797 ENPP6, LOC107986204
    nsv6314260complex chromosomal rearrangement3nstd102humanUncertain significance GRCh37 chr11: 87,665,403-87,665,403 , GRCh37 chr11: 87,665,449-87,665,449 , GRCh38.p12 chr11: 87,954,511-87,954,511 , GRCh38.p12 chr11: 87,954,557-87,954,557 , GRCh38.p12 chr2: 185,168,383-185,168,383 , GRCh38.p12 chr2: 185,168,415-185,168,415 , GRCh38.p12 chr2: 185,174,384-185,174,384 , GRCh38.p12 chr2: 185,174,733-185,174,733 , GRCh37 chr2: 186,033,110-186,033,110 , GRCh37 chr2: 186,033,142-186,033,142 , GRCh37 chr2: 186,039,111-186,039,111 , GRCh37 chr2: 186,039,460-186,039,460 RAB38, LOC105373781
    nsv6314555complex chromosomal rearrangement7nstd102humanPathogenic GRCh37 chr8: 65,187,723-65,187,723 , GRCh37 chr8: 68,393,835-68,393,835 , GRCh37 chr8: 65,187,602-65,187,602 , GRCh37 chr8: 68,393,684-68,393,684 , GRCh37 chr8: 70,181,445-70,181,445 , GRCh37 chr8: 70,181,450-70,181,450 , GRCh37 chr8: 54,482,780-54,482,780 , GRCh37 chr8: 54,482,780-54,482,780 , GRCh37 chr10: 2,187,369-2,187,369 , GRCh37 chr10: 2,059,927-2,059,927 , GRCh37 chr10: 2,059,928-2,059,928 , GRCh37 chr10: 9,592,748-9,592,748 , GRCh37 chr10: 9,592,706-9,592,706 , GRCh37 chr10: 2,187,182-2,187,182 , GRCh38.p12 chr10: 2,017,734-2,017,734 , GRCh38.p12 chr10: 2,144,988-2,144,988 , GRCh38.p12 chr10: 9,550,785-9,550,785 , GRCh38.p12 chr10: 2,145,175-2,145,175 , GRCh38.p12 chr10: 9,550,743-9,550,743 , GRCh38.p12 chr10: 2,017,733-2,017,733 , GRCh38.p12 chr8: 64,275,045-64,275,045 , GRCh38.p12 chr8: 67,481,449-67,481,449 , GRCh38.p12 chr8: 67,481,600-67,481,600 , GRCh38.p12 chr8: 69,269,210-69,269,210 , GRCh38.p12 chr8: 69,269,215-69,269,215 , GRCh38.p12 chr8: 64,275,166-64,275,166 , GRCh38.p12 chr8: 53,570,220-53,570,220 , GRCh38.p12 chr8: 53,570,220-53,570,220 LINC02663, ARFGEF1-DT, 2 more genes
    nsv6314541complex chromosomal rearrangement9nstd102humanPathogenic GRCh37 chr4: 173,991,710-173,991,710 , GRCh37 chr4: 179,499,907-179,499,907 , GRCh37 chr4: 179,498,840-179,498,840 , GRCh37 chr4: 173,991,974-173,991,974 , GRCh37 chr5: 34,389,491-34,389,491 , GRCh37 chr5: 6,819,324-6,819,324 , GRCh37 chr5: 62,181,285-62,181,285 , GRCh37 chr5: 62,181,297-62,181,297 , GRCh37 chr5: 6,819,330-6,819,330 , GRCh37 chr5: 34,389,486-34,389,486 , GRCh37 chr6: 15,947,640-15,947,640 , GRCh37 chr6: 15,947,649-15,947,649 , GRCh37 chr6: 16,375,942-16,375,942 , GRCh37 chr6: 20,761,251-20,761,251 , GRCh37 chr6: 16,375,942-16,375,942 , GRCh37 chr6: 20,727,413-20,727,413 , GRCh37 chr6: 20,727,421-20,727,421 , GRCh37 chr6: 20,761,289-20,761,289 , GRCh38.p12 chr4: 173,070,559-173,070,559 , GRCh38.p12 chr4: 173,070,823-173,070,823 , GRCh38.p12 chr4: 178,577,686-178,577,686 , GRCh38.p12 chr4: 178,578,753-178,578,753 , GRCh38.p12 chr5: 34,389,386-34,389,386 , GRCh38.p12 chr5: 34,389,381-34,389,381 , GRCh38.p12 chr5: 62,885,458-62,885,458 , GRCh38.p12 chr5: 6,819,217-6,819,217 , GRCh38.p12 chr5: 62,885,470-62,885,470 , GRCh38.p12 chr5: 6,819,211-6,819,211 , GRCh38.p12 chr6: 15,947,409-15,947,409 , GRCh38.p12 chr6: 16,375,711-16,375,711 , GRCh38.p12 chr6: 16,375,711-16,375,711 , GRCh38.p12 chr6: 20,727,190-20,727,190 , GRCh38.p12 chr6: 20,761,020-20,761,020 , GRCh38.p12 chr6: 15,947,418-15,947,418 , GRCh38.p12 chr6: 20,727,182-20,727,182 , GRCh38.p12 chr6: 20,761,058-20,761,058 ATXN1, CDKAL1, 1 more genes
    nsv6314498complex chromosomal rearrangement5nstd102humanPathogenic GRCh37 chr5: 93,026,965-93,026,965 , GRCh37 chr5: 93,258,066-93,258,066 , GRCh37 chr5: 153,852,297-153,852,297 , GRCh37 chr5: 153,351,885-153,351,885 , GRCh37 chr5: 153,351,885-153,351,885 , GRCh37 chr5: 153,852,297-153,852,297 , GRCh37 chr5: 93,026,965-93,026,965 , GRCh37 chr5: 92,616,397-92,616,397 , GRCh37 chr5: 92,616,397-92,616,397 , GRCh37 chr5: 93,258,062-93,258,062 , GRCh38.p12 chr5: 93,691,259-93,691,259 , GRCh38.p12 chr5: 154,472,737-154,472,737 , GRCh38.p12 chr5: 93,922,357-93,922,357 , GRCh38.p12 chr5: 153,972,325-153,972,325 , GRCh38.p12 chr5: 93,691,259-93,691,259 , GRCh38.p12 chr5: 93,922,361-93,922,361 , GRCh38.p12 chr5: 93,280,691-93,280,691 , GRCh38.p12 chr5: 93,280,691-93,280,691 , GRCh38.p12 chr5: 153,972,325-153,972,325 , GRCh38.p12 chr5: 154,472,737-154,472,737 LOC107983980, ARB2A, 1 more genes
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