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Items: 1 to 20 of 397

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7029625copy number variation1nstd229human GRCh38 chr20: 32,311,436-32,311,742 , GRCh37.p13 chr20: 30,899,239-30,899,545 KIF3B
    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
    nsv7021991copy number variation1nstd229human GRCh38 chr20: 32,324,480-32,327,187 , GRCh37.p13 chr20: 30,912,283-30,914,990 KIF3B
    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
    nsv6599724inversion1nstd223human GRCh38 chr20: 32,290,864-32,291,619 , GRCh37.p13 chr20: 30,878,667-30,879,422 KIF3B
    nsv6598095inversion1nstd223human GRCh38 chr20: 32,328,306-32,329,039 , GRCh37.p13 chr20: 30,916,109-30,916,842 KIF3B
    nsv6597975inversion1nstd223human GRCh38 chr20: 32,297,934-32,299,627 , GRCh37.p13 chr20: 30,885,737-30,887,430 KIF3B
    nsv6597355inversion1nstd223human GRCh38 chr20: 32,291,896-32,292,392 , GRCh37.p13 chr20: 30,879,699-30,880,195 KIF3B
    nsv6597179inversion1nstd223human GRCh38 chr20: 32,305,143-32,305,594 , GRCh37.p13 chr20: 30,892,946-30,893,397 KIF3B
    nsv6596438inversion1nstd223human GRCh38 chr20: 32,307,773-32,308,457 , GRCh37.p13 chr20: 30,895,576-30,896,260 KIF3B
    nsv6595981inversion1nstd223human GRCh38 chr20: 32,324,898-32,325,402 , GRCh37.p13 chr20: 30,912,701-30,913,205 KIF3B
    nsv6519638copy number variation1nstd223human GRCh38 chr20: 32,280,685-32,281,602 , GRCh37.p13 chr20: 30,868,488-30,869,405 KIF3B
    nsv6517319copy number variation1nstd223human GRCh38 chr20: 32,277,501-32,278,100 , GRCh37.p13 chr20: 30,865,304-30,865,903 KIF3B
    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
    nsv6251386mobile element insertion1nstd215human GRCh38 chr20: 32,322,982-32,322,982 , GRCh37.p13 chr20: 30,910,785-30,910,785 KIF3B
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