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Items: 1 to 20 of 155

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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
    nsv6897418copy number variation1nstd229human GRCh38 chr10: 117,175,317-117,264,604 , GRCh37.p13 chr10: 118,934,828-119,024,115 RPL12P26, SLC18A2-AS1, 2 more genes
    nsv6897177copy number variation1nstd229human GRCh38 chr10: 117,263,127-117,266,896 , GRCh37.p13 chr10: 119,022,638-119,026,407 SLC18A2
    nsv6882713copy number variation1nstd229human GRCh38 chr10: 117,263,286-117,265,444 , GRCh37.p13 chr10: 119,022,797-119,024,955 SLC18A2
    nsv6879491copy number variation1nstd229human GRCh38 chr10: 117,204,575-117,253,030 , GRCh37.p13 chr10: 118,964,086-119,012,541 KCNK18, SLC18A2, 1 more genes
    nsv6449087copy number variation1nstd223human GRCh38 chr10: 117,275,288-117,275,298 , GRCh37.p13 chr10: 119,034,799-119,034,809 SLC18A2, PDZD8
    nsv6439077copy number variation1nstd223human GRCh38 chr10: 117,254,056-117,255,613 , GRCh37.p13 chr10: 119,013,567-119,015,124 SLC18A2
    nsv6439069copy number variation1nstd223human GRCh38 chr10: 117,263,286-117,265,444 , GRCh37.p13 chr10: 119,022,797-119,024,955 SLC18A2
    nsv6314129copy number variation1nstd102humanPathogenic GRCh37 chr10: 117,019,650-125,217,066 , GRCh38.p12 chr10: 115,260,173-123,457,550 PDZD8, MIR3663HG, 122 more genes
    nsv6314085copy number variation1nstd102humanPathogenic GRCh37 chr10: 108,455,687-135,427,143 , GRCh38.p12 chr10: 106,695,929-133,613,639 LOC107984268, DPYSL4, 379 more genes
    nsv6290269copy number variation1nstd102humanUncertain significance GRCh37 chr10: 118,891,670-122,349,064 , GRCh38.p12 chr10: 117,132,159-120,589,552 MCMBP, PDZD8, 54 more genes
    nsv6132021copy number variation1nstd213human GRCh37 chr10: 118,730,000-119,070,001 , GRCh38.p12 chr10: 116,970,489-117,310,490 SLC18A2, VAX1, 7 more genes
    nsv6131932copy number variation1nstd213human GRCh37 chr10: 115,960,000-125,870,001 , GRCh38.p12 chr10: 114,200,241-124,109,956 ACADSB, DMBT1, 148 more genes
    nsv6131853copy number variation1nstd213human GRCh37 chr10: 118,780,000-119,090,001 , GRCh38.p12 chr10: 117,020,489-117,330,490 SLC18A2, VAX1, 7 more genes
    nsv6131766copy number variation1nstd213human GRCh37 chr10: 116,010,000-125,870,001 , GRCh38.p12 chr10: 114,250,241-124,109,956 ACADSB, DMBT1, 146 more genes
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5974801inversion1nstd209human GRCh38 chr10: 116,446,135-119,236,441 , GRCh37.p13 chr10: 118,205,647-120,995,953 EMX2, PRLHR, 48 more genes
    nsv5500547copy number variation1nstd206human GRCh38 chr10: 117,061,313-117,431,413 , GRCh37.p13 chr10: 118,820,824-119,190,924 SLC18A2, VAX1, 7 more genes
    nsv5499665copy number variation1nstd206human GRCh38 chr10: 117,269,062-117,269,133 , GRCh37.p13 chr10: 119,028,573-119,028,644 SLC18A2
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