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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5604721insertion1nstd207human GRCh38 chr1: 160,178,216-160,178,216 , GRCh37.p13 chr1: 160,148,006-160,148,006 ATP1A4
    nsv5580327copy number variation1nstd207human GRCh38 chr1: 160,170,134-160,170,269 , GRCh37.p13 chr1: 160,139,924-160,140,059 ATP1A4
    nsv5431538copy number variation1nstd206human GRCh38 chr1: 160,162,831-160,162,917 , GRCh37.p13 chr1: 160,132,621-160,132,707 ATP1A4
    nsv5420595copy number variation1nstd206human GRCh38 chr1: 160,165,283-160,166,076 , GRCh37.p13 chr1: 160,135,073-160,135,866 ATP1A4
    nsv5418150copy number variation1nstd206human GRCh38 chr1: 160,178,083-160,178,441 , GRCh37.p13 chr1: 160,147,873-160,148,231 ATP1A4
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5192142mobile element insertion1nstd203human GRCh38 chr1: 160,160,857-160,160,869 , GRCh37.p13 chr1: 160,130,647-160,130,659 ATP1A4
    nsv4897726copy number variation1nstd200human GRCh38 chr1: 160,163,434-160,164,617 , GRCh37.p13 chr1: 160,133,224-160,134,407 ATP1A4
    nsv4784439copy number variation1nstd200human GRCh37 chr1: 160,135,288-160,135,815 , GRCh38.p12 chr1: 160,165,498-160,166,025 ATP1A4
    nsv4784438copy number variation1nstd200human GRCh37 chr1: 160,125,741-160,135,286 , GRCh38.p12 chr1: 160,155,951-160,165,496 ATP1A4
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4579768copy number variation1nstd183human GRCh37 chr1: 160,133,965-160,134,349 , GRCh38.p12 chr1: 160,164,175-160,164,559 ATP1A4
    nsv4450412copy number variation1nstd102humanPathogenic GRCh37 chr1: 157,321,299-167,391,423 , GRCh38.p12 chr1: 157,351,509-167,422,186 FCGR3B, SLAMF9, 302 more genes
    nsv4450321copy number variation1nstd102humanUncertain significance GRCh37 chr1: 159,808,188-161,011,163 , GRCh38.p12 chr1: 159,838,398-161,041,373 LOC107985216, PPIAP37, 50 more genes
    nsv4327204inversion1nstd166human GRCh37.p13 chr1: 156,223,026-186,411,081 , GRCh38.p12 chr1: 156,253,235-186,441,949 , FASLG, 707 more genes
    nsv4070666copy number variation1nstd166human GRCh37.p13 chr1: 160,128,923-160,132,466 , GRCh38.p12 chr1: 160,159,133-160,162,676 ATP1A4
    nsv4065091copy number variation1nstd166human GRCh37.p13 chr1: 160,147,873-160,148,191 , GRCh38.p12 chr1: 160,178,083-160,178,401 ATP1A4
    nsv4063300copy number variation1nstd166human GRCh37.p13 chr1: 160,126,287-160,127,254 , GRCh38.p12 chr1: 160,156,497-160,157,464 ATP1A4
    nsv4058136copy number variation1nstd166human GRCh37.p13 chr1: 160,135,319-160,135,786 , GRCh38.p12 chr1: 160,165,529-160,165,996 ATP1A4
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