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Items: 1 to 20 of 1974

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv507853sequence alteration2nstd49human NCBI35 chr17: 59,795,793-59,801,793 , GRCh37.p13 chr17|NW_003315947.1: 168,540-178,805 , GRCh38.p12 chr17: 64,364,693-64,374,958 PECAM1
    nsv510379sequence alteration2nstd49human NCBI35 chr14: 48,556,521-48,562,521 , GRCh37.p13 chr14: 49,486,771-49,492,771 , GRCh38.p12 chr14: 49,017,568-49,026,053 LOC105378178
    nsv507259sequence alteration4nstd49human NCBI35 chr5: 68,954,453-68,960,453 , GRCh37.p13 chr5|NW_003315917.2: 928,764-935,285 , GRCh37.p13 chr5: 68,918,697-68,924,697 , GRCh38.p12 chr5: 69,622,870-69,628,870 , GRCh38.p12 chr5|NW_003315917.2: 928,764-935,285 NAIPP3, NAIPP1
    nsv507337sequence alteration3nstd49human NCBI35 chr6: 70,949,093-70,955,093 , GRCh37.p13 chr6: 70,892,372-70,898,372 , GRCh38.p12 chr6: 70,182,480-70,188,668 COL19A1
    nsv507460sequence alteration2nstd49human NCBI35 chr8: 39,188,097-39,194,097 , GRCh37.p13 chr8: 39,068,940-39,074,940 , GRCh38.p12 chr8: 39,211,421-39,217,421 , GRCh38.p12 chr8|NT_187577.1: 117,112-123,129 ADAM32
    nsv507441sequence alteration2nstd49human NCBI35 chr8: 9,009,496-9,015,496 , GRCh37.p13 chr8: 8,972,086-8,978,086 , GRCh38.p12 chr8: 9,114,576-9,120,576 , GRCh38.p12 chr8|NW_018654717.1: 4,231,075-4,237,081 LOC112268402
    nsv510024sequence alteration2nstd49human NCBI35 chr6: 32,884,679-32,890,679 , GRCh37.p13 chr6|NT_113891.2: 4,222,290-4,227,231 , GRCh37.p13 chr6|NT_167245.1: 4,059,279-4,064,227 , GRCh37.p13 chr6|NT_167247.1: 4,113,601-4,119,602 , GRCh37.p13 chr6|NT_167249.1: 4,208,690-4,213,634 , GRCh37.p13 chr6|NT_167244.1: 4,064,920-4,069,864 , GRCh37.p13 chr6: 32,776,701-32,782,701 , GRCh38.p12 chr6: 32,808,924-32,814,924 , GRCh38.p12 chr6|NT_167247.2: 4,108,016-4,114,017 , GRCh38.p12 chr6|NT_167249.2: 4,209,392-4,214,336 , GRCh38.p12 chr6|NT_167245.2: 4,053,694-4,058,642 , GRCh38.p12 chr6|NT_113891.3: 4,222,184-4,227,125 , GRCh38.p12 chr6|NT_167246.2: 4,228,277-4,231,330 , GRCh38.p12 chr6|NT_167244.2: 4,115,004-4,119,948 HLA-DOB
    nsv510567sequence alteration3nstd49human NCBI35 chrX: 149,614,208-149,620,208 , GRCh37.p13 chrX|NW_004070890.2: 6,299,565-6,305,565 , GRCh37.p13 chrX: 149,943,640-149,949,640 , GRCh38.p12 chrX: 150,775,167-150,781,167 CD99L2
    nsv510566sequence alteration1nstd49human NCBI35 chrX: 148,496,644-148,502,644 , GRCh37.p13 chrX|NW_004070890.2: 5,212,352-5,218,352 , GRCh37.p13 chrX: 148,769,620-148,775,614 , GRCh38.p12 chrX: 149,687,954-149,693,954 MAGEA11
    nsv510553sequence alteration2nstd49human NCBI35 chrX: 117,424,323-117,430,323 , GRCh37.p13 chrX: 117,642,441-117,648,441 , GRCh38.p12 chrX: 118,508,478-118,514,478 DOCK11
    nsv510549sequence alteration1nstd49human NCBI35 chrX: 95,885,838-95,891,838 , GRCh37.p13 chrX: 96,079,693-96,085,693 , GRCh38.p12 chrX: 96,824,694-96,830,694 DIAPH2
    nsv510548sequence alteration2nstd49human NCBI35 chrX: 91,488,243-91,494,243 , GRCh37.p13 chrX: 91,682,098-91,688,098 , GRCh38.p12 chrX: 92,427,099-92,433,099 PCDH11X
    nsv510545sequence alteration2nstd49human NCBI35 chrX: 85,063,496-85,069,496 , GRCh37.p13 chrX: 85,257,351-85,263,351 , GRCh38.p12 chrX: 86,002,347-86,008,347 CHM
    nsv510544sequence alteration1nstd49human NCBI35 chrX: 79,286,081-79,292,081 , GRCh37.p13 chrX: 79,479,936-79,485,936 , GRCh38.p12 chrX: 80,224,437-80,230,437 CHMP1B2P
    nsv510538sequence alteration2nstd49human NCBI35 chrX: 56,469,245-56,475,245 , GRCh37.p13 chrX: 56,586,224-56,592,224 , GRCh38.p12 chrX: 56,559,791-56,565,791 UBQLN2
    nsv510532sequence alteration4nstd49human NCBI35 chrX: 30,332,582-30,338,582 , GRCh37.p13 chrX: 30,572,925-30,578,925 , GRCh38.p12 chrX: 30,554,808-30,560,808 TASL
    nsv510525sequence alteration2nstd49human NCBI35 chrX: 12,354,842-12,360,842 , GRCh37.p13 chrX: 12,595,185-12,601,185 , GRCh38.p12 chrX: 12,577,066-12,583,066 FRMPD4
    nsv510523sequence alteration1nstd49human NCBI35 chrX: 5,888,984-5,894,984 , GRCh37.p13 chrX: 6,029,248-6,035,248 , GRCh38.p12 chrX: 6,111,207-6,117,207 NLGN4X
    nsv510521sequence alteration4nstd49human NCBI35 chrX: 2,699,376-2,705,376 , GRCh37.p13 chrX: 2,706,015-2,712,015 , GRCh38.p12 chrX: 2,787,974-2,793,974 XG
    nsv510516sequence alteration1nstd49human NCBI35 chr22: 35,466,610-35,472,610 , GRCh37.p13 chr22: 37,142,110-37,148,110 , GRCh38.p12 chr22: 36,746,066-36,752,066 CACNG2-DT
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