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Items: 1 to 20 of 201

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114236mobile element insertion1nstd186human GRCh37 chr19: 51,860,645-51,860,696 , GRCh38.p12 chr19: 51,357,391-51,357,442 ETFB
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5967812insertion1nstd209human GRCh38 chr19: 51,357,375-51,357,375 , GRCh37.p13 chr19: 51,860,629-51,860,629 ETFB
    nsv5703356mobile element insertion2nstd211human GRCh38 chr19: 51,357,391-51,357,391 , GRCh37.p13 chr19: 51,860,645-51,860,645 ETFB
    nsv5657845insertion1nstd207human GRCh38 chr19: 51,345,993-51,345,993 , GRCh37.p13 chr19: 51,849,247-51,849,247 ETFB
    nsv5657052insertion1nstd207human GRCh38 chr19: 51,345,973-51,345,973 , GRCh37.p13 chr19: 51,849,227-51,849,227 ETFB
    nsv5653537insertion1nstd207human GRCh38 chr19: 51,346,272-51,346,272 , GRCh37.p13 chr19: 51,849,526-51,849,526 ETFB
    nsv5652712insertion1nstd207human GRCh38 chr19: 51,345,864-51,345,864 , GRCh37.p13 chr19: 51,849,118-51,849,118 ETFB
    nsv5644784insertion1nstd207human GRCh38 chr19: 51,357,375-51,357,375 , GRCh37.p13 chr19: 51,860,629-51,860,629 ETFB
    nsv5598105copy number variation1nstd207human GRCh38 chr19: 51,353,421-51,353,494 , GRCh37.p13 chr19: 51,856,675-51,856,748 ETFB
    nsv5594876copy number variation1nstd207human GRCh38 chr19: 51,353,689-51,353,799 , GRCh37.p13 chr19: 51,856,943-51,857,053 ETFB
    nsv5427190mobile element insertion1nstd206human GRCh38 chr19: 51,357,391-51,357,442 , GRCh37.p13 chr19: 51,860,645-51,860,696 ETFB
    nsv5179651mobile element insertion1nstd203human GRCh38 chr19: 51,357,377-51,357,389 , GRCh37.p13 chr19: 51,860,631-51,860,643 ETFB
    nsv5179181mobile element insertion1nstd203human GRCh38 chr19: 51,357,373-51,357,391 , GRCh37.p13 chr19: 51,860,627-51,860,645 ETFB
    nsv5176960mobile element insertion1nstd203human GRCh38 chr19: 51,357,380-51,357,391 , GRCh37.p13 chr19: 51,860,634-51,860,645 ETFB
    nsv5175710mobile element insertion1nstd203human GRCh38 chr19: 51,357,353-51,357,375 , GRCh37.p13 chr19: 51,860,607-51,860,629 ETFB
    nsv5174876mobile element insertion1nstd203human GRCh38 chr19: 51,357,375-51,357,389 , GRCh37.p13 chr19: 51,860,629-51,860,643 ETFB
    nsv5173772mobile element insertion1nstd203human GRCh38 chr19: 51,357,381-51,357,391 , GRCh37.p13 chr19: 51,860,635-51,860,645 ETFB
    nsv5171323mobile element insertion1nstd203human GRCh38 chr19: 51,357,378-51,357,387 , GRCh37.p13 chr19: 51,860,632-51,860,641 ETFB
    nsv5171128mobile element insertion1nstd203human GRCh38 chr19: 51,357,383-51,357,389 , GRCh37.p13 chr19: 51,860,637-51,860,643 ETFB
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