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Items: 1 to 20 of 114

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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
    nsv5714246mobile element insertion2nstd211human GRCh38 chr12: 56,359,468-56,359,468 , GRCh37.p13 chr12: 56,753,252-56,753,252 APOF, STAT2
    nsv5646476insertion1nstd207human GRCh38 chr12: 56,359,452-56,359,452 , GRCh37.p13 chr12: 56,753,236-56,753,236 APOF, STAT2
    nsv5418137mobile element insertion1nstd206human GRCh38 chr12: 56,359,468-56,359,519 , GRCh37.p13 chr12: 56,753,252-56,753,303 STAT2, APOF
    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
    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
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4721642insertion1nstd186human GRCh37 chr12: 56,753,236-56,753,236 , GRCh38.p12 chr12: 56,359,452-56,359,452 APOF, STAT2
    nsv4691256mobile element insertion1nstd186human GRCh37 chr12: 56,753,252-56,753,252 , GRCh38.p12 chr12: 56,359,468-56,359,468 STAT2, APOF
    nsv4675143copy number variation1nstd102humanPathogenic GRCh37 chr12: 55,552,371-62,126,304 , GRCh38.p12 chr12: 55,158,587-61,732,523 OR6C71P, METTL1, 183 more genes
    nsv4612228copy number variation1nstd183human GRCh37 chr12: 56,739,950-56,785,153 , GRCh38.p12 chr12: 56,346,166-56,391,369 LOC100128676, RNU7-40P, 3 more genes
    nsv4539080insertion1nstd166human GRCh37.p13 chr12: 56,753,236-56,753,236 , GRCh38.p12 chr12: 56,359,452-56,359,452 STAT2, APOF
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