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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137190copy number variation1nstd102humanLikely benign GRCh38 chr20: 32,231,112-32,231,177 , GRCh37 chr20: 30,818,915-30,818,980 POFUT1
    nsv7065834inversion1nstd229human GRCh38 chr20: 32,176,022-32,321,070 , GRCh37.p13 chr20: 30,763,825-30,908,873 PLAGL2, KIF3B, 3 more genes
    nsv7059980inversion1nstd229human GRCh38 chr20: 30,656,049-33,860,963 , GRCh37.p13 chr20: 29,803,910-32,448,769 NECAB3, EFCAB8, 98 more genes
    nsv7032154copy number variation1nstd229human GRCh38 chr20: 32,208,162-32,209,311 , GRCh37.p13 chr20: 30,795,965-30,797,114 PLAGL2, POFUT1
    nsv7031428copy number variation1nstd229human GRCh38 chr20: 32,222,394-32,225,612 , GRCh37.p13 chr20: 30,810,197-30,813,415 POFUT1
    nsv7030915copy number variation1nstd229human GRCh38 chr20: 32,212,728-32,247,029 , GRCh37.p13 chr20: 30,800,531-30,834,832 POFUT1, MIR1825
    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
    nsv7022919copy number variation1nstd229human GRCh38 chr20: 32,237,429-32,357,170 , GRCh37.p13 chr20: 30,825,232-30,944,973 POFUT1, ASXL1, 2 more genes
    nsv7019138copy number variation1nstd229human GRCh38 chr20: 32,219,301-32,221,800 , GRCh37.p13 chr20: 30,807,104-30,809,603 POFUT1
    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
    nsv6532315copy number variation1nstd223human GRCh38 chr20: 32,212,728-32,247,006 , GRCh37.p13 chr20: 30,800,531-30,834,809 POFUT1, MIR1825
    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
    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
    nsv6225748copy number variation1nstd214human GRCh38 chr20: 32,231,111-32,231,176 , GRCh37.p13 chr20: 30,818,914-30,818,979 POFUT1
    nsv6134286copy number variation1nstd213human GRCh37 chr20: 30,610,000-30,990,001 , GRCh38.p12 chr20: 32,022,197-32,402,198 HCK, TM9SF4, 9 more genes
    nsv6124888copy number variation1nstd186human GRCh37 chr20: 30,818,917-30,818,980 , GRCh38.p12 chr20: 32,231,114-32,231,177 POFUT1
    nsv6047422copy number variation1nstd212human GRCh38 chr20: 32,231,111-32,231,177 , GRCh37.p13 chr20: 30,818,914-30,818,980 POFUT1
    nsv5966597copy number variation1nstd209human GRCh38 chr20: 32,231,111-32,231,176 , GRCh37.p13 chr20: 30,818,914-30,818,979 POFUT1
    nsv5961933copy number variation1nstd209human GRCh38 chr20: 32,225,233-32,225,531 , GRCh37.p13 chr20: 30,813,036-30,813,334 POFUT1
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