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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7031041copy number variation1nstd229human GRCh38 chr20: 34,045,788-34,051,768 , GRCh37.p13 chr20: 32,633,594-32,639,574 RALY, MIR4755
    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
    nsv7020533copy number variation1nstd229human GRCh38 chr20: 34,047,280-34,053,433 , GRCh37.p13 chr20: 32,635,086-32,641,239 MIR4755, RALY
    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
    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
    nsv6133807copy number variation1nstd213human GRCh37 chr20: 32,330,000-32,810,001 , GRCh38.p12 chr20: 33,742,194-34,222,195 XPOTP1, RALY, 11 more genes
    nsv5954434copy number variation1nstd209human GRCh38 chr20: 34,044,011-34,048,119 , GRCh37.p13 chr20: 32,631,817-32,635,925 RALY, MIR4755
    nsv5884085copy number variation1nstd209human GRCh38 chr20: 34,043,991-34,047,590 , GRCh37.p13 chr20: 32,631,797-32,635,396 MIR4755, RALY
    nsv5533344copy number variation1nstd206human GRCh38 chr20: 34,048,916-34,049,168 , GRCh37.p13 chr20: 32,636,722-32,636,974 MIR4755, RALY
    nsv5022411copy number variation1nstd200human GRCh38 chr20: 34,048,937-34,049,148 , GRCh37.p13 chr20: 32,636,743-32,636,954 MIR4755, RALY
    nsv5022343copy number variation1nstd200human GRCh38 chr20: 32,602,560-45,347,064 , GRCh37.p13 chr20: 31,190,362-43,975,704 , SNHG11, 286 more genes
    nsv5022342copy number variation1nstd200human GRCh38 chr20: 32,576,247-46,538,786 , GRCh37.p13 chr20: 31,164,049-45,167,425 , NECAB3, 350 more genes
    nsv5022326copy number variation1nstd200human GRCh38 chr20: 32,216,214-44,981,731 , GRCh37.p13 chr20: 30,804,017-43,610,372 , HNF4A, 279 more genes
    nsv4868593copy number variation1nstd200human GRCh37 chr20: 31,164,049-45,167,425 , GRCh38.p12 chr20: 32,576,247-46,538,786 , MMP24-AS1-EDEM2, 350 more genes
    nsv4868578copy number variation1nstd200human GRCh37 chr20: 30,804,017-43,610,372 , GRCh38.p12 chr20: 32,216,214-44,981,731 , SNORA71C, 279 more genes
    nsv4676132copy number variation1nstd102humanUncertain significance GRCh37 chr20: 31,966,407-33,169,058 , GRCh38.p12 chr20: 33,378,601-34,581,254 MAP1LC3A, PXMP4, 28 more genes
    nsv4457806copy number variation1nstd102humanPathogenic GRCh37 chr20: 29,833,608-35,087,952 , GRCh38.p12 chr20: 31,245,805-36,459,549 EFCAB8, C20orf203, 162 more genes
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