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Items: 1 to 20 of 166

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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
    nsv7036435copy number variation1nstd229human GRCh38 chr20: 33,195,276-33,195,490 , GRCh37.p13 chr20: 31,783,082-31,783,296 BPIFA4P
    nsv7035533copy number variation1nstd229human GRCh38 chr20: 33,185,640-33,195,003 , GRCh37.p13 chr20: 31,773,446-31,782,809 SOCS2P1, BPIFA4P
    nsv7029285copy number variation1nstd229human GRCh38 chr20: 33,189,423-33,197,136 , GRCh37.p13 chr20: 31,777,229-31,784,942 BPIFA4P
    nsv7028368copy number variation1nstd229human GRCh38 chr20: 31,579,910-33,642,127 , GRCh37.p13 chr20: 30,167,713-32,229,933 PLAGL2, BPIFB4, 57 more genes
    nsv7023214copy number variation1nstd229human GRCh38 chr20: 33,171,743-33,245,380 , GRCh37.p13 chr20: 31,759,549-31,833,186 BPIFA1, BPIFA4P, 4 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
    nsv7020395copy number variation1nstd229human GRCh38 chr20: 33,180,552-33,192,611 , GRCh37.p13 chr20: 31,768,358-31,780,417 SOCS2P1, BPIFA4P, 1 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
    nsv6533912copy number variation1nstd223human GRCh38 chr20: 33,185,620-33,195,002 , GRCh37.p13 chr20: 31,773,426-31,782,808 SOCS2P1, BPIFA4P
    nsv6518591copy number variation1nstd223human GRCh38 chr20: 33,192,398-33,194,582 , GRCh37.p13 chr20: 31,780,204-31,782,388 BPIFA4P
    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
    nsv6134287copy number variation1nstd213human GRCh37 chr20: 31,520,000-31,940,001 , GRCh38.p12 chr20: 32,932,194-33,352,195 BPIFA3, PUDPP3, 17 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
    nsv5022378copy number variation1nstd200human GRCh38 chr20: 33,198,266-33,198,422 , GRCh37.p13 chr20: 31,786,072-31,786,228 BPIFA4P
    nsv5022377copy number variation1nstd200human GRCh38 chr20: 33,195,515-33,198,062 , GRCh37.p13 chr20: 31,783,321-31,785,868 BPIFA4P
    nsv5022376copy number variation1nstd200human GRCh38 chr20: 33,192,398-33,194,582 , GRCh37.p13 chr20: 31,780,204-31,782,388 BPIFA4P
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