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Items: 1 to 20 of 267

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148267copy number variation1nstd102humanPathogenic GRCh38 chr20: 87,153-23,635,465 , GRCh37.p13 chr20: 67,794-23,616,102 KRT18P3, RSPO4, 413 more genes
    nsv7073483inversion1nstd229human GRCh38 chr20: 10,258,890-10,258,991 , GRCh37.p13 chr20: 10,239,538-10,239,639 SNAP25
    nsv7065782inversion1nstd229human GRCh38 chr20: 10,247,273-10,247,311 , GRCh37.p13 chr20: 10,227,921-10,227,959 SNAP25
    nsv7037000copy number variation1nstd229human GRCh38 chr20: 10,233,258-10,233,401 , GRCh37.p13 chr20: 10,213,906-10,214,049 SNAP25
    nsv7036855copy number variation1nstd229human GRCh38 chr20: 10,234,350-10,235,005 , GRCh37.p13 chr20: 10,214,998-10,215,653 SNAP25
    nsv7032827copy number variation1nstd229human GRCh38 chr20: 10,228,140-10,261,992 , GRCh37.p13 chr20: 10,208,788-10,242,640 SNAP25
    nsv7031361copy number variation1nstd229human GRCh38 chr20: 10,264,425-10,269,978 , GRCh37.p13 chr20: 10,245,073-10,250,626 SNAP25
    nsv7030920copy number variation1nstd229human GRCh38 chr20: 10,265,110-10,272,855 , GRCh37.p13 chr20: 10,245,758-10,253,503 SNAP25
    nsv7030872copy number variation1nstd229human GRCh38 chr20: 10,263,701-10,272,800 , GRCh37.p13 chr20: 10,244,349-10,253,448 SNAP25
    nsv7024576copy number variation1nstd229human GRCh38 chr20: 10,281,074-10,282,447 , GRCh37.p13 chr20: 10,261,722-10,263,095 SNAP25
    nsv7022729copy number variation1nstd229human GRCh38 chr20: 7,235,562-10,519,088 , GRCh37.p13 chr20: 7,216,209-10,499,736 MKKS, PHKBP1, 30 more genes
    nsv7022067copy number variation1nstd229human GRCh38 chr20: 7,868,752-11,491,709 , GRCh37.p13 chr20: 7,849,399-11,472,357 LOC339593, LOC105372522, 36 more genes
    nsv6597926inversion1nstd223human GRCh38 chr20: 10,288,121-10,288,228 , GRCh37.p13 chr20: 10,268,769-10,268,876 SNAP25
    nsv6535122copy number variation1nstd223human GRCh38 chr20: 10,265,110-10,272,846 , GRCh37.p13 chr20: 10,245,758-10,253,494 SNAP25
    nsv6535064copy number variation1nstd223human GRCh38 chr20: 10,257,628-10,257,800 , GRCh37.p13 chr20: 10,238,276-10,238,448 SNAP25
    nsv6534438copy number variation1nstd223human GRCh38 chr20: 10,249,684-10,250,163 , GRCh37.p13 chr20: 10,230,332-10,230,811 SNAP25
    nsv6525155copy number variation1nstd223human GRCh38 chr20: 10,285,701-10,287,500 , GRCh37.p13 chr20: 10,266,349-10,268,148 SNAP25
    nsv6520634copy number variation1nstd223human GRCh38 chr20: 10,283,700-10,284,449 , GRCh37.p13 chr20: 10,264,348-10,265,097 SNAP25
    nsv6315526copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,178,539-11,848,383 , GRCh38.p12 chr20: 3,197,893-11,867,735 LRRN4, MCM8-AS1, 129 more genes
    nsv6311245copy number variation1nstd102humanUncertain significance GRCh37 chr20: 7,812,350-10,654,278 , GRCh38.p12 chr20: 7,831,703-10,673,630 LOC100421490, RNU105B, 27 more genes
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