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Items: 1 to 20 of 214

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5639815insertion1nstd207human GRCh38 chr10: 125,824,766-125,824,766 , GRCh37.p13 chr10: 127,513,335-127,513,335 BCCIP
    nsv5512945copy number variation1nstd206human GRCh38 chr10: 125,824,766-125,825,185 , GRCh37.p13 chr10: 127,513,335-127,513,754 BCCIP
    nsv5499312copy number variation1nstd206human GRCh38 chr10: 125,834,897-125,835,345 , GRCh37.p13 chr10: 127,523,466-127,523,914 DHX32, BCCIP
    nsv5497298copy number variation1nstd206human GRCh38 chr10: 125,834,857-125,835,394 , GRCh37.p13 chr10: 127,523,426-127,523,963 DHX32, BCCIP
    nsv5308911copy number variation1nstd204human GRCh38.p13 chr10: 125,824,766-125,825,185 , GRCh37.p13 chr10: 127,513,335-127,513,754 BCCIP
    nsv5303475copy number variation1nstd204human GRCh37.p13 chr10: 127,523,523-127,524,100 , GRCh38.p13 chr10: 125,834,954-125,835,531 DHX32, BCCIP
    nsv4983979copy number variation1nstd200human GRCh38 chr10: 125,824,766-125,825,185 , GRCh37.p13 chr10: 127,513,335-127,513,754 BCCIP
    nsv4983971copy number variation1nstd200human GRCh38 chr10: 125,039,754-126,334,238 , GRCh37.p13 chr10: 126,728,323-128,022,807 , ADAM12, 28 more genes
    nsv4977434copy number variation1nstd200human GRCh38 chr10: 125,833,075-125,833,888 , GRCh37.p13 chr10: 127,521,644-127,522,457 BCCIP
    nsv4848474copy number variation1nstd200human GRCh37 chr10: 127,513,335-127,513,754 , GRCh38.p12 chr10: 125,824,766-125,825,185 BCCIP
    nsv4842625copy number variation1nstd200human GRCh37 chr10: 127,535,643-127,536,631 , GRCh38.p12 chr10: 125,847,074-125,848,062 DHX32, BCCIP
    nsv4830032copy number variation1nstd200human GRCh37 chr10: 127,521,644-127,522,457 , GRCh38.p12 chr10: 125,833,075-125,833,888 BCCIP
    nsv4709148tandem duplication2nstd195human GRCh37 chr10: 127,513,335-127,513,336 , GRCh38.p12 chr10: 125,824,766-125,824,767 BCCIP
    nsv4675991copy number variation1nstd102humanPathogenic GRCh37 chr10: 119,996,339-135,427,143 , GRCh38.p12 chr10: 118,236,827-133,613,639 STK32C, LOC105378542, 237 more genes
    nsv4648926copy number variation3nstd186human GRCh37 chr10: 127,513,335-127,513,754 , GRCh38.p12 chr10: 125,824,766-125,825,185 BCCIP
    nsv4527816copy number variation1nstd166human GRCh37.p13 chr10: 127,512,324-127,512,391 , GRCh38.p12 chr10: 125,823,755-125,823,822 UROS, BCCIP
    nsv4527611copy number variation1nstd166human GRCh37.p13 chr10: 127,513,335-127,513,754 , GRCh38.p12 chr10: 125,824,766-125,825,185 BCCIP
    nsv4497001mobile element insertion1nstd166human GRCh37.p13 chr10: 127,527,376-127,527,376 , GRCh38.p12 chr10: 125,838,807-125,838,807 DHX32, BCCIP
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