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Items: 1 to 20 of 484

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7035888copy number variation1nstd229human GRCh38 chr20: 34,200,948-34,201,020 , GRCh37.p13 chr20: 32,788,754-32,788,826 ASIP
    nsv7028071copy number variation1nstd229human GRCh38 chr20: 34,200,901-34,214,700 , GRCh37.p13 chr20: 32,788,707-32,802,506 ASIP, XPOTP1
    nsv7027638copy number variation1nstd229human GRCh38 chr20: 34,185,219-34,185,246 , GRCh37.p13 chr20: 32,773,025-32,773,052 ASIP
    nsv7023561copy number variation1nstd229human GRCh38 chr20: 34,184,368-34,188,427 , GRCh37.p13 chr20: 32,772,174-32,776,233 ASIP
    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
    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
    nsv6530216copy number variation1nstd223human GRCh38 chr20: 34,114,358-34,192,321 , GRCh37.p13 chr20: 32,702,164-32,780,127 RPS2P1, ASIP
    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
    nsv6520320copy number variation1nstd223human GRCh38 chr20: 34,196,215-34,198,102 , GRCh37.p13 chr20: 32,784,021-32,785,908 ASIP
    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
    nsv6311078copy number variation1nstd102humanPathogenic GRCh37 chr20: 31,189,994-34,287,210 , GRCh38.p12 chr20: 32,602,192-35,699,288 EDEM2, EIF2S2, 93 more genes
    nsv6291578copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 18,665,879-33,903,216 , GRCh38.p12 chr20: 18,685,235-35,315,413 AHCY, ASIP, 330 more genes
    nsv6282588copy number variation1nstd214human GRCh38 chr20: 34,200,948-34,201,023 , GRCh37.p13 chr20: 32,788,754-32,788,829 ASIP
    nsv6251401mobile element insertion1nstd215human GRCh38 chr20: 34,243,491-34,243,491 , GRCh37.p13 chr20: 32,831,297-32,831,297 AHCY, ASIP
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