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Items: 1 to 20 of 316

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973174insertion1nstd209human GRCh38 chr22: 42,818,816-42,818,816 , GRCh37.p13 chr22: 43,214,822-43,214,822 ARFGAP3
    nsv5952717copy number variation1nstd209human GRCh38 chr22: 42,798,273-42,798,453 , GRCh37.p13 chr22: 43,194,279-43,194,459 ARFGAP3
    nsv5869434copy number variation1nstd209human GRCh38 chr22: 42,797,352-42,798,451 , GRCh37.p13 chr22: 43,193,358-43,194,457 ARFGAP3
    nsv5673276copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,440,000-43,780,000 , GRCh38.p12 chr22: 42,043,996-43,383,994 RPL5P34, ARFGAP3, 48 more genes
    nsv5671235insertion1nstd207human GRCh38 chr22: 42,829,299-42,829,299 , GRCh37.p13 chr22: 43,225,305-43,225,305 ARFGAP3
    nsv5667751insertion1nstd207human GRCh38 chr22: 42,818,816-42,818,816 , GRCh37.p13 chr22: 43,214,822-43,214,822 ARFGAP3
    nsv5548772copy number variation1nstd206human GRCh38 chr22: 42,798,273-42,798,454 , GRCh37.p13 chr22: 43,194,279-43,194,460 ARFGAP3
    nsv5542802insertion1nstd206human GRCh38 chr22: 42,818,816-42,818,816 , GRCh37.p13 chr22: 43,214,822-43,214,822 ARFGAP3
    nsv5381149copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,333,802-51,195,728 , GRCh38.p12 chr22: 41,937,798-50,757,300 WBP2NL, RN7SKP80, 210 more genes
    nsv5381088copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,356,886-43,684,002 , GRCh38.p12 chr22: 41,960,882-43,287,996 CYP2D8P, SCUBE1, 49 more genes
    nsv5324135copy number variation1nstd204human GRCh38.p13 chr22: 42,798,268-42,798,459 , GRCh37.p13 chr22: 43,194,274-43,194,465 ARFGAP3
    nsv5178516mobile element insertion1nstd203human GRCh38 chr22: 42,818,821-42,818,830 , GRCh37.p13 chr22: 43,214,827-43,214,836 ARFGAP3
    nsv5176686mobile element insertion1nstd203human GRCh38 chr22: 42,818,818-42,818,830 , GRCh37.p13 chr22: 43,214,824-43,214,836 ARFGAP3
    nsv5176031mobile element insertion1nstd203human GRCh38 chr22: 42,818,824-42,818,830 , GRCh37.p13 chr22: 43,214,830-43,214,836 ARFGAP3
    nsv5174622mobile element insertion1nstd203human GRCh38 chr22: 42,818,815-42,818,830 , GRCh37.p13 chr22: 43,214,821-43,214,836 ARFGAP3
    nsv5171874mobile element insertion1nstd203human GRCh38 chr22: 42,818,820-42,818,828 , GRCh37.p13 chr22: 43,214,826-43,214,834 ARFGAP3
    nsv5170080mobile element insertion1nstd203human GRCh38 chr22: 42,818,822-42,818,830 , GRCh37.p13 chr22: 43,214,828-43,214,836 ARFGAP3
    nsv5168640mobile element insertion1nstd203human GRCh38 chr22: 42,818,825-42,818,830 , GRCh37.p13 chr22: 43,214,831-43,214,836 ARFGAP3
    nsv5167078mobile element insertion1nstd203human GRCh38 chr22: 42,818,819-42,818,830 , GRCh37.p13 chr22: 43,214,825-43,214,836 ARFGAP3
    nsv5166435mobile element insertion1nstd203human GRCh38 chr22: 42,818,817-42,818,830 , GRCh37.p13 chr22: 43,214,823-43,214,836 ARFGAP3
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