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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5969119insertion1nstd209human GRCh38 chr12: 56,359,452-56,359,452 , GRCh37.p13 chr12: 56,753,236-56,753,236 STAT2, APOF
    nsv5867107copy number variation1nstd209human GRCh38 chr12: 56,350,278-56,351,777 , GRCh37.p13 chr12: 56,744,062-56,745,561 RNU7-40P, STAT2
    nsv5858605copy number variation1nstd209human GRCh38 chr12: 56,346,209-56,348,008 , GRCh37.p13 chr12: 56,739,993-56,741,792 STAT2
    nsv5714246mobile element insertion2nstd211human GRCh38 chr12: 56,359,468-56,359,468 , GRCh37.p13 chr12: 56,753,252-56,753,252 APOF, STAT2
    nsv5700963mobile element insertion1nstd211human GRCh38 chr12: 56,352,349-56,352,349 , GRCh37.p13 chr12: 56,746,133-56,746,133 STAT2, RNU7-40P
    nsv5662163insertion1nstd207human GRCh38 chr12: 56,345,524-56,345,524 , GRCh37.p13 chr12: 56,739,308-56,739,308 STAT2
    nsv5646476insertion1nstd207human GRCh38 chr12: 56,359,452-56,359,452 , GRCh37.p13 chr12: 56,753,236-56,753,236 APOF, STAT2
    nsv5542528insertion1nstd206human GRCh38 chr12: 56,345,536-56,345,561 , GRCh37.p13 chr12: 56,739,320-56,739,345 STAT2
    nsv5418137mobile element insertion1nstd206human GRCh38 chr12: 56,359,468-56,359,519 , GRCh37.p13 chr12: 56,753,252-56,753,303 STAT2, APOF
    nsv5268818copy number variation1nstd204human GRCh38.p13 chr12: 56,345,509-56,353,628 , GRCh37.p13 chr12: 56,739,293-56,747,412 STAT2, RNU7-40P
    nsv5131999mobile element insertion1nstd203human GRCh38 chr12: 56,359,456-56,359,468 , GRCh37.p13 chr12: 56,753,240-56,753,252 STAT2, APOF
    nsv5130135mobile element insertion1nstd203human GRCh38 chr12: 56,359,468-56,359,468 , GRCh37.p13 chr12: 56,753,252-56,753,252 STAT2, APOF
    nsv5128142mobile element insertion1nstd203human GRCh38 chr12: 56,359,458-56,359,468 , GRCh37.p13 chr12: 56,753,242-56,753,252 APOF, STAT2
    nsv5124057mobile element insertion1nstd203human GRCh38 chr12: 56,359,452-56,359,468 , GRCh37.p13 chr12: 56,753,236-56,753,252 STAT2, APOF
    nsv5120948mobile element insertion1nstd203human GRCh38 chr12: 56,359,457-56,359,468 , GRCh37.p13 chr12: 56,753,241-56,753,252 STAT2, APOF
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv4985647copy number variation1nstd200human GRCh38 chr12: 56,297,696-56,345,186 , GRCh37.p13 chr12: 56,691,480-56,738,970 CNPY2-AS1, CS, 4 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4756148insertion1nstd199human GRCh37 chr12: 56,753,245-56,753,245 , GRCh38.p12 chr12: 56,359,461-56,359,461 APOF, STAT2
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