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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5946632copy number variation1nstd209human GRCh38 chr19: 15,623,516-15,623,577 , GRCh37.p13 chr19: 15,734,326-15,734,387 CYP4F8
    nsv5661722insertion1nstd207human GRCh38 chr19: 15,616,094-15,616,094 , GRCh37.p13 chr19: 15,726,905-15,726,905 CYP4F8
    nsv5653434insertion1nstd207human GRCh38 chr19: 15,630,047-15,630,047 , GRCh37.p13 chr19: 15,740,857-15,740,857 CYP4F8
    nsv5645729insertion1nstd207human GRCh38 chr19: 15,616,212-15,616,212 , GRCh37.p13 chr19: 15,727,023-15,727,023 CYP4F8
    nsv5602684copy number variation1nstd207human GRCh38 chr19: 15,623,516-15,623,577 , GRCh37.p13 chr19: 15,734,326-15,734,387 CYP4F8
    nsv5528871copy number variation1nstd206human GRCh38 chr19: 15,623,517-15,623,578 , GRCh37.p13 chr19: 15,734,327-15,734,388 CYP4F8
    nsv5328440copy number variation1nstd204human GRCh38.p13 chr19: 15,623,517-15,623,578 , GRCh37.p13 chr19: 15,734,327-15,734,388 CYP4F8
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5012034copy number variation1nstd200human GRCh38 chr19: 15,623,517-15,623,578 , GRCh37.p13 chr19: 15,734,327-15,734,388 CYP4F8
    nsv4860475copy number variation1nstd200human GRCh37 chr19: 15,734,327-15,734,388 , GRCh38.p12 chr19: 15,623,517-15,623,578 CYP4F8
    nsv4759905insertion1nstd199human GRCh37 chr19: 15,726,721-15,726,721 , GRCh38.p12 chr19: 15,615,910-15,615,910 CYP4F8
    nsv4747366copy number variation1nstd199human GRCh37 chr19: 15,734,326-15,734,387 , GRCh38.p12 chr19: 15,623,516-15,623,577 CYP4F8
    nsv4729750copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,286,624-20,956,753 , GRCh38.p12 chr19: 14,175,812-20,773,947 LOC105372309, RAB8A, 269 more genes
    nsv4651081copy number variation1nstd186human GRCh37 chr19: 15,734,326-15,734,388 , GRCh38.p12 chr19: 15,623,516-15,623,578 CYP4F8
    nsv4635009copy number variation4nstd186human GRCh37 chr19: 15,734,327-15,734,388 , GRCh38.p12 chr19: 15,623,517-15,623,578 CYP4F8
    nsv4628505copy number variation1nstd183human GRCh37 chr19: 15,422,142-16,172,833 , GRCh38.p12 chr19: 15,311,331-16,062,023 , CYP4F8, 36 more genes
    nsv4576476mobile element insertion1nstd166human GRCh37.p13 chr19: 15,735,984-15,735,984 , GRCh38.p12 chr19: 15,625,174-15,625,174 CYP4F8
    nsv4551504insertion1nstd166human GRCh37.p13 chr19: 15,740,857-15,740,857 , GRCh38.p12 chr19: 15,630,047-15,630,047 CYP4F8
    nsv4534948copy number variation1nstd166human GRCh37.p13 chr19: 15,734,326-15,734,388 , GRCh38.p12 chr19: 15,623,516-15,623,578 CYP4F8
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