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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7093904copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,344,461-105,992,004 , GRCh38.p12 chr10: 97,584,704-104,232,246 ABCC2, LBX1-AS1, 160 more genes
    nsv7061391inversion1nstd229human GRCh38 chr10: 100,357,388-105,969,995 , GRCh37.p13 chr10: 102,117,145-107,729,753 , CALHM1, 127 more genes
    nsv6895230copy number variation1nstd229human GRCh38 chr10: 103,230,955-103,592,585 , GRCh37.p13 chr10: 104,990,712-105,352,342 RPEL1, CALHM3, 12 more genes
    nsv6892128copy number variation1nstd229human GRCh38 chr10: 103,387,326-103,408,595 , GRCh37.p13 chr10: 105,147,083-105,168,352 MIR1307, TAF5, 2 more genes
    nsv6891788copy number variation1nstd229human GRCh38 chr10: 103,205,994-103,520,342 , GRCh37.p13 chr10: 104,965,751-105,280,099 ATP5MK, PDCD11, 12 more genes
    nsv6880434copy number variation1nstd229human GRCh38 chr10: 103,302,516-106,977,869 , GRCh37.p13 chr10: 105,062,273-108,737,627 RNU11-3P, GSTO2, 48 more genes
    nsv6637523copy number variation1nstd102humanUncertain significance GRCh37 chr10: 105,015,345-105,911,204 , GRCh38.p12 chr10: 103,255,588-104,151,446 PCGF6, INA, 20 more genes
    nsv6594978inversion1nstd223human GRCh38 chr10: 103,205,613-103,520,468 , GRCh37.p13 chr10: 104,965,370-105,280,225 ST13P13, CALHM1, 12 more genes
    nsv6585036inversion1nstd223human GRCh38 chr10: 103,372,459-103,372,747 , GRCh37.p13 chr10: 105,132,216-105,132,504 TAF5
    nsv6580477inversion1nstd223human GRCh38 chr10: 103,366,774-103,367,113 , GRCh37.p13 chr10: 105,126,531-105,126,870 TAF5
    nsv6313941copy number variation1nstd102humanUncertain significance GRCh37 chr10: 105,064,606-105,508,469 , GRCh38.p12 chr10: 103,304,849-103,748,711 CALHM3, NEURL1, 11 more genes
    nsv6131926copy number variation1nstd213human GRCh37 chr10: 103,560,000-105,280,001 , GRCh38.p12 chr10: 101,800,243-103,520,244 ARL3, CYP17A1, 56 more genes
    nsv6020296copy number variation1nstd212human GRCh38 chr10: 103,376,241-103,376,345 , GRCh37.p13 chr10: 105,135,998-105,136,102 TAF5
    nsv6010670copy number variation1nstd212human GRCh38 chr10: 103,366,391-103,366,785 , GRCh37.p13 chr10: 105,126,148-105,126,542 TAF5
    nsv5909873copy number variation1nstd209human GRCh38 chr10: 103,354,716-103,423,522 , GRCh37.p13 chr10: 105,114,473-105,183,279 TAF5, MIR1307, 2 more genes
    nsv5908075copy number variation1nstd209human GRCh38 chr10: 103,366,364-103,366,761 , GRCh37.p13 chr10: 105,126,121-105,126,518 TAF5
    nsv5860008copy number variation1nstd209human GRCh38 chr10: 103,355,875-103,367,091 , GRCh37.p13 chr10: 105,115,632-105,126,848 TAF5
    nsv5850763copy number variation1nstd209human GRCh38 chr10: 103,365,192-103,379,229 , GRCh37.p13 chr10: 105,124,949-105,138,986 TAF5
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