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Items: 1 to 20 of 253

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5904127copy number variation1nstd209human GRCh38 chr3: 9,996,659-11,875,087 , GRCh37.p13 chr3: 10,038,343-11,916,561 , EMC3, 35 more genes
    nsv5901270copy number variation1nstd209human GRCh38 chr3: 10,048,544-11,870,471 , GRCh37.p13 chr3: 10,090,228-11,911,945 , SLC6A11, 29 more genes
    nsv5896636copy number variation1nstd209human GRCh38 chr3: 10,148,303-10,149,150 , GRCh37.p13 chr3: 10,189,987-10,190,834 VHL
    nsv5891525copy number variation1nstd209human GRCh38 chr3: 9,996,478-11,874,953 , GRCh37.p13 chr3: 10,038,162-11,916,427 , TATDN2, 35 more genes
    nsv5834476copy number variation1nstd209human GRCh38 chr3: 10,148,319-10,149,329 , GRCh37.p13 chr3: 10,190,003-10,191,013 VHL
    nsv5673717copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr3: 10,183,532-10,188,330 , GRCh38.p12 chr3: 10,141,848-10,146,646 VHL
    nsv5581871copy number variation1nstd207human GRCh38 chr3: 10,148,384-10,149,181 , GRCh37.p13 chr3: 10,190,068-10,190,865 VHL
    nsv5564434copy number variation1nstd102humanUncertain significance GRCh37 chr3: 10,183,522-10,188,330 , GRCh38.p12 chr3: 10,141,838-10,146,646 VHL
    nsv5446789copy number variation1nstd206human GRCh38 chr3: 10,147,424-10,148,701 , GRCh37.p13 chr3: 10,189,108-10,190,385 VHL
    nsv5435784copy number variation1nstd206human GRCh38 chr3: 10,148,395-10,149,138 , GRCh37.p13 chr3: 10,190,079-10,190,822 VHL
    nsv5381364copy number variation1nstd102humanUncertain significance GRCh37 chr3: 9,976,103-10,191,669 , GRCh38.p12 chr3: 9,934,419-10,149,985 CYCSP10, MARK2P2, 13 more genes
    nsv5381357copy number variation1nstd102humanUncertain significance GRCh37 chr3: 10,103,825-10,184,708 , GRCh38.p12 chr3: 10,062,141-10,143,024 FANCD2, FANCD2OS, 2 more genes
    nsv5351438translocation1nstd200human GRCh38 chr3: 10,147,733-10,147,733 , GRCh38 chr3: 10,147,671-10,147,671 , GRCh37.p13 chr3: 10,189,417-10,189,417 , GRCh37.p13 chr3: 10,189,355-10,189,355 VHL
    nsv5313845copy number variation1nstd204human GRCh38.p13 chr3: 10,148,358-10,149,167 , GRCh37.p13 chr3: 10,190,042-10,190,851 VHL
    nsv5311699copy number variation1nstd204human GRCh38.p13 chr3: 9,776,127-10,149,069 , GRCh37.p13 chr3: 9,817,811-10,190,753 EMC3, CYCSP11, 25 more genes
    nsv5301514copy number variation1nstd204human GRCh38.p13 chr3: 10,147,614-10,148,513 , GRCh37.p13 chr3: 10,189,298-10,190,197 VHL
    nsv5205129copy number variation1nstd204human GRCh38.p13 chr3: 9,776,301-10,148,700 , GRCh37.p13 chr3: 9,817,985-10,190,384 JAGN1, TTLL3, 25 more genes
    nsv5200353copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,190,251-10,200,086 , GRCh38 chr3: 10,148,567-10,158,402 VHL
    nsv5200352copy number variation1nstd102humanPathogenic GRCh38 chr3: 10,148,558-10,152,733 , GRCh37 chr3: 10,190,242-10,194,417 VHL
    nsv5200351copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,190,210-10,200,045 , GRCh38 chr3: 10,148,526-10,158,361 VHL
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