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Items: 1 to 20 of 216

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112688copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144 RNU4-62P, MTCO1P29, 169 more genes
    nsv5960091insertion1nstd209human GRCh38 chr3: 120,706,613-120,706,613 , GRCh37.p13 chr3: 120,425,460-120,425,460 RABL3
    nsv5907046copy number variation1nstd209human GRCh38 chr3: 120,684,480-120,684,777 , GRCh37.p13 chr3: 120,403,327-120,403,624 RABL3
    nsv5721666mobile element insertion2nstd211human GRCh38 chr3: 120,699,127-120,699,127 , GRCh37.p13 chr3: 120,417,974-120,417,974 RABL3
    nsv5687465mobile element insertion2nstd211human GRCh38 chr3: 120,706,628-120,706,628 , GRCh37.p13 chr3: 120,425,475-120,425,475 RABL3
    nsv5616967insertion1nstd207human GRCh38 chr3: 120,706,613-120,706,613 , GRCh37.p13 chr3: 120,425,460-120,425,460 RABL3
    nsv5562069mobile element insertion1nstd206human GRCh38 chr3: 120,699,127-120,699,178 , GRCh37.p13 chr3: 120,417,974-120,418,025 RABL3
    nsv5397943mobile element insertion1nstd206human GRCh38 chr3: 120,706,628-120,706,679 , GRCh37.p13 chr3: 120,425,475-120,425,526 RABL3
    nsv5361879translocation1nstd200human GRCh38 chr3: 120,765,086-120,765,086 , GRCh38 chr3: 120,729,530-120,729,530 , GRCh37.p13 chr3: 120,483,933-120,483,933 , GRCh37.p13 chr3: 120,448,377-120,448,377 RABL3, GTF2E1
    nsv5173172mobile element insertion1nstd203human GRCh38 chr3: 120,699,116-120,699,127 , GRCh37.p13 chr3: 120,417,963-120,417,974 RABL3
    nsv5093964mobile element insertion1nstd203human GRCh38 chr3: 120,706,620-120,706,628 , GRCh37.p13 chr3: 120,425,467-120,425,475 RABL3
    nsv5090462mobile element insertion1nstd203human GRCh38 chr3: 120,706,617-120,706,624 , GRCh37.p13 chr3: 120,425,464-120,425,471 RABL3
    nsv5090310mobile element insertion1nstd203human GRCh38 chr3: 120,706,616-120,706,628 , GRCh37.p13 chr3: 120,425,463-120,425,475 RABL3
    nsv5090022mobile element insertion1nstd203human GRCh38 chr3: 120,706,618-120,706,628 , GRCh37.p13 chr3: 120,425,465-120,425,475 RABL3
    nsv5085920mobile element insertion1nstd203human GRCh38 chr3: 120,706,613-120,706,628 , GRCh37.p13 chr3: 120,425,460-120,425,475 RABL3
    nsv5083273mobile element insertion1nstd203human GRCh38 chr3: 120,706,612-120,706,628 , GRCh37.p13 chr3: 120,425,459-120,425,475 RABL3
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5031637inversion1nstd200human GRCh38 chr3: 112,181,184-125,673,487 , GRCh37.p13 chr3: 111,900,031-125,392,331 , ARHGAP31, 218 more genes
    nsv4919812copy number variation1nstd200human GRCh38 chr3: 120,711,275-120,713,610 , GRCh37.p13 chr3: 120,430,122-120,432,457 RABL3
    nsv4919809copy number variation1nstd200human GRCh38 chr3: 120,532,331-120,850,460 , GRCh37.p13 chr3: 120,251,178-120,569,307 GTF2E1, HGD, 6 more genes
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