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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099235copy number variation1nstd231human GRCh38.p12 chr1: 154,116,919-155,715,830 , GRCh37 chr1: 154,089,395-155,685,621 ADAR, CHRNB2, 80 more genes
    nsv7057328inversion1nstd229human GRCh38 chr1: 154,938,555-155,849,490 , GRCh37.p13 chr1: 154,911,031-155,819,281 ENTREP3, YY1AP1, 57 more genes
    nsv7056666inversion1nstd229human GRCh38 chr1: 151,403,323-155,722,147 , GRCh37.p13 chr1: 151,375,799-155,691,938 ILF2, SPRR2C, 219 more genes
    nsv7042502inversion1nstd229human GRCh38 chr1: 150,301,267-155,517,761 , GRCh37.p13 chr1: 150,440,214-155,487,552 LINGO4, CELF3, 268 more genes
    nsv7041246inversion1nstd229human GRCh38 chr1: 153,232,460-155,277,038 , GRCh37.p13 chr1: 153,204,936-155,246,829 INTS3, GBA1LP, 111 more genes
    nsv7041047inversion1nstd229human GRCh38 chr1: 154,596,558-159,585,927 , GRCh37.p13 chr1: 154,569,034-159,555,717 ADAR, SNORA80E, 204 more genes
    nsv6327858copy number variation1nstd223human GRCh38 chr1: 155,271,518-155,272,343 , GRCh37.p13 chr1: 155,241,309-155,242,134 CLK2
    nsv6310678copy number variation4nstd102humanUncertain significance GRCh37 chr1: 149,895,434-156,851,434 , GRCh38.p12 chr1: 149,923,542-156,881,642 PRPF3, KHDC4, 352 more genes
    nsv6310523copy number variation1nstd102humanUncertain significance GRCh37 chr1: 154,141,761-156,851,434 , GRCh38.p12 chr1: 154,169,285-156,881,642 MIR555, CFAP141, 135 more genes
    nsv6138309copy number variation1nstd206human GRCh38 chr1: 155,270,000-155,276,587 , GRCh37.p13 chr1: 155,239,791-155,246,378 CLK2, HCN3
    nsv6133737copy number variation1nstd213human GRCh37 chr1: 153,820,000-155,320,001 , GRCh38.p12 chr1: 153,847,524-155,350,210 GBA1LP, PKLR, 81 more genes
    nsv6133560copy number variation1nstd213human GRCh37 chr1: 153,460,000-155,250,001 , GRCh38.p12 chr1: 153,487,524-155,280,210 CKS1B, ILF2, 97 more genes
    nsv6133504copy number variation1nstd213human GRCh37 chr1: 154,420,000-155,500,001 , GRCh38.p12 chr1: 154,447,524-155,530,210 EFNA1, GBA1LP, 51 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4673954copy number variation1nstd102humanUncertain significance GRCh37 chr1: 154,898,854-155,242,457 , GRCh38.p12 chr1: 154,926,378-155,272,666 GBA1LP, PBXIP1, 31 more genes
    nsv4579739copy number variation2nstd183human GRCh37 chr1: 155,227,059-155,262,674 , GRCh38.p12 chr1: 155,257,268-155,292,883 , GRCh38.p12 chr1|NW_003315906.1: 62,291-97,906 PKLR, HCN3, 2 more genes
    nsv4397258copy number variation1nstd174human GRCh37 chr1: 155,180,791-155,234,821 , GRCh38.p12 chr1: 155,211,000-155,265,030 , GRCh38.p12 chr1|NW_003315906.1: 1-70,053 CLK2, GBA1, 6 more genes
    nsv3970158insertion1nstd168human GRCh38 chr1: 155,233,397-155,264,748 , GRCh37.p13 chr1: 155,203,188-155,234,539 CLK2, GBA1, 3 more genes
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