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Items: 1 to 20 of 385

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145263insertion1nstd232human GRCh37.p13 chr20: 32,879,339-32,879,339 , GRCh38.p12 chr20: 34,291,533-34,291,533 AHCY
    nsv7144186copy number variation1nstd232human GRCh37.p13 chr20: 32,878,443-32,878,534 , GRCh38.p12 chr20: 34,290,637-34,290,728 AHCY
    nsv7142265insertion1nstd232human GRCh37.p13 chr20: 32,873,442-32,873,442 , GRCh38.p12 chr20: 34,285,636-34,285,636 AHCY
    nsv7095890copy number variation1nstd102humanUncertain significance GRCh37 chr20: 32,868,840-33,033,286 , GRCh38.p12 chr20: 34,281,034-34,445,481 ITCH, CDC42P1, 1 more genes
    nsv7076246inversion1nstd229human GRCh38 chr20: 34,251,218-34,251,257 , GRCh37.p13 chr20: 32,839,024-32,839,063 AHCY, ASIP
    nsv7060285inversion1nstd229human GRCh38 chr20: 34,194,327-34,356,240 , GRCh37.p13 chr20: 32,782,133-32,944,046 ASIP, XPOTP1, 2 more genes
    nsv7033764copy number variation1nstd229human GRCh38 chr20: 34,271,884-34,279,752 , GRCh37.p13 chr20: 32,859,690-32,867,558 AHCY
    nsv7032230copy number variation1nstd229human GRCh38 chr20: 34,308,043-34,314,848 , GRCh37.p13 chr20: 32,895,849-32,902,654 AHCY
    nsv7023000copy number variation1nstd229human GRCh38 chr20: 34,120,053-34,253,634 , GRCh37.p13 chr20: 32,707,859-32,841,440 LOC729557, ASIP, 3 more genes
    nsv7022457copy number variation1nstd229human GRCh38 chr20: 34,255,908-34,328,728 , GRCh37.p13 chr20: 32,843,714-32,916,534 ASIP, AHCY
    nsv7021198copy number variation1nstd229human GRCh38 chr20: 33,145,032-41,995,765 , GRCh37.p13 chr20: 31,732,838-40,624,405 PXMP4, RPL12P11, 199 more genes
    nsv7019370copy number variation1nstd229human GRCh38 chr20: 34,286,701-34,290,800 , GRCh37.p13 chr20: 32,874,507-32,878,606 AHCY
    nsv6637725copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,833,535-34,815,537 , GRCh38.p12 chr20: 31,245,732-36,227,615 AHCY, ASIP, 160 more genes
    nsv6637546copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,652,122-35,603,726 , GRCh38.p12 chr20: 30,417,446-36,975,323 AHCY, ASIP, 195 more genes
    nsv6626689copy number variation1nstd224human GRCh37 chr20: 32,738,612-32,913,534 , GRCh38.p12 chr20: 34,150,806-34,325,728 LOC729557, AHCY, 2 more genes
    nsv6599911inversion1nstd223human GRCh38 chr20: 34,297,295-34,297,951 , GRCh37.p13 chr20: 32,885,101-32,885,757 AHCY
    nsv6533943copy number variation1nstd223human GRCh38 chr20: 34,277,699-34,279,311 , GRCh37.p13 chr20: 32,865,505-32,867,117 AHCY
    nsv6525013copy number variation1nstd223human GRCh38 chr20: 34,242,485-34,245,641 , GRCh37.p13 chr20: 32,830,291-32,833,447 LOC729557, AHCY, 1 more genes
    nsv6521472copy number variation1nstd223human GRCh38 chr20: 34,271,879-34,279,751 , GRCh37.p13 chr20: 32,859,685-32,867,557 AHCY
    nsv6313956copy number variation1nstd102humanPathogenic GRCh37 chr20: 25,442,597-33,761,550 , GRCh38.p12 chr20: 25,461,961-35,173,747 LOC105372586, RNU6-384P, 193 more genes
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