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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099226copy number variation1nstd231human GRCh38.p12 chr1: 115,063,638-119,984,872 , GRCh37 chr1: 115,606,259-120,527,495 ATP1A1, CASQ2, 103 more genes
    nsv7095241copy number variation1nstd102humanPathogenic GRCh37 chr1: 119,466,351-120,286,570 , GRCh38.p12 chr1: 118,923,728-119,743,947 HAO2-IT1, LINC01780, 29 more genes
    nsv7093235copy number variation1nstd102humanPathogenic GRCh38 chr1: 119,421,844-119,422,250 , GRCh37 chr1: 119,964,467-119,964,873 HSD3B2
    nsv7057703inversion1nstd229human GRCh38 chr1: 119,295,932-119,453,572 , GRCh37.p13 chr1: 119,838,555-119,996,195 LINC01780, RNU1-75P, 5 more genes
    nsv7056415inversion1nstd229human GRCh38 chr1: 119,421,087-119,445,794 , GRCh37.p13 chr1: 119,963,710-119,988,417 HSD3B2, GAPDHP74, 1 more genes
    nsv7050357inversion1nstd229human GRCh38 chr1: 119,422,548-119,445,805 , GRCh37.p13 chr1: 119,965,171-119,988,428 HSD3B2, GAPDHP74, 1 more genes
    nsv7047805inversion1nstd229human GRCh38 chr1: 119,209,133-119,576,834 , GRCh37.p13 chr1: 119,751,756-120,119,457 HSD3BP4, RNU1-75P, 17 more genes
    nsv6640996copy number variation1nstd229human GRCh38 chr1: 119,180,006-119,885,056 , GRCh37.p13 chr1: 119,722,629-120,427,679 PHGDH, NOTCH2P1, 28 more genes
    nsv6640971copy number variation1nstd229human GRCh38 chr1: 119,413,529-119,413,589 , GRCh37.p13 chr1: 119,956,152-119,956,212 HSD3B2
    nsv6640876copy number variation1nstd229human GRCh38 chr1: 119,294,157-119,747,268 , GRCh37.p13 chr1: 119,836,780-120,289,891 ZNF697, HSD3BP3, 21 more genes
    nsv6637125copy number variation1nstd102humanUncertain significance GRCh37 chr1: 119,836,835-120,151,604 , GRCh38.p12 chr1: 119,294,212-119,608,981 HSD3BP4, GAPDHP33, 17 more genes
    nsv6335312copy number variation1nstd223human GRCh38 chr1: 119,414,029-119,414,618 , GRCh37.p13 chr1: 119,956,652-119,957,241 HSD3B2
    nsv6332826copy number variation1nstd223human GRCh38 chr1: 119,386,345-119,599,790 , GRCh37.p13 chr1: 119,928,968-120,142,413 HAO2, GAPDHP32, 14 more genes
    nsv6313671copy number variation1nstd102humanPathogenic GRCh37 chr1: 111,647,582-121,343,783 , GRCh38.p12 chr1: 111,104,960-121,601,985 GAPDHP23, RNA5SP56, 243 more genes
    nsv6310720copy number variation1nstd102humanPathogenic GRCh37 chr1: 119,964,988-119,988,456 , GRCh38.p12 chr1: 119,422,365-119,445,833 HSD3BP2, HSD3B2, 1 more genes
    nsv6310719copy number variation1nstd102humanUncertain significance GRCh37 chr1: 119,618,953-120,311,467 , GRCh38.p12 chr1: 119,076,330-119,768,844 LOC105378937, HMGCS2, 27 more genes
    nsv6310669copy number variation2nstd102humanUncertain significance GRCh37 chr1: 119,427,355-120,529,725 , GRCh38.p12 chr1: 118,884,732-119,987,102 NOTCH2P1, NOTCH2, 36 more genes
    nsv6290447copy number variation1nstd102humanUncertain significance GRCh37 chr1: 119,584,796-120,527,495 , GRCh38.p12 chr1: 119,042,173-119,984,872 RBMX2P3, NOTCH2P1, 34 more genes
    nsv6156450copy number variation1nstd214human GRCh38 chr1: 119,421,405-119,421,476 , GRCh37.p13 chr1: 119,964,028-119,964,099 HSD3B2
    nsv6150560copy number variation1nstd214human GRCh38 chr1: 119,421,419-119,421,476 , GRCh37.p13 chr1: 119,964,042-119,964,099 HSD3B2
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