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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7059980inversion1nstd229human GRCh38 chr20: 30,656,049-33,860,963 , GRCh37.p13 chr20: 29,803,910-32,448,769 NECAB3, EFCAB8, 98 more genes
    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
    nsv7019769copy number variation1nstd229human GRCh38 chr20: 33,313,823-33,665,850 , GRCh37.p13 chr20: 31,901,629-32,253,656 BPIFB5P, CDK5RAP1, 6 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
    nsv6626341copy number variation1nstd224human GRCh37 chr20: 32,162,037-32,369,354 , GRCh38.p12 chr20: 33,574,231-33,781,548 E2F1, CBFA2T2, 6 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
    nsv6133806copy number variation1nstd213human GRCh37 chr20: 30,990,000-32,330,001 , GRCh38.p12 chr20: 32,402,197-33,742,195 SNTA1, ZNF341, 36 more genes
    nsv5871253copy number variation1nstd209human GRCh38 chr20: 33,663,453-33,664,552 , GRCh37.p13 chr20: 32,251,259-32,252,358 C20orf144, NECAB3
    nsv5700729mobile element insertion1nstd211human GRCh38 chr20: 33,662,964-33,662,964 , GRCh37.p13 chr20: 32,250,770-32,250,770 C20orf144, NECAB3
    nsv5426896mobile element insertion1nstd206human GRCh38 chr20: 33,662,964-33,663,015 , GRCh37.p13 chr20: 32,250,770-32,250,821 NECAB3, C20orf144
    nsv5025519copy number variation1nstd200human GRCh38 chr20: 33,313,823-33,665,851 , GRCh37.p13 chr20: 31,901,629-32,253,657 CBFA2T2, C20orf144, 6 more genes
    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
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