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Items: 1 to 20 of 241

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6126996copy number variation1nstd186human GRCh37 chr20: 10,213,906-10,214,049 , GRCh38.p12 chr20: 10,233,258-10,233,401 SNAP25
    nsv5944974copy number variation1nstd209human GRCh38 chr20: 10,269,203-10,270,491 , GRCh37.p13 chr20: 10,249,851-10,251,139 SNAP25
    nsv5935715copy number variation1nstd209human GRCh38 chr20: 10,233,258-10,233,395 , GRCh37.p13 chr20: 10,213,906-10,214,043 SNAP25
    nsv5934528copy number variation1nstd209human GRCh38 chr20: 10,260,436-10,260,506 , GRCh37.p13 chr20: 10,241,084-10,241,154 SNAP25
    nsv5877773copy number variation1nstd209human GRCh38 chr20: 10,269,361-10,270,560 , GRCh37.p13 chr20: 10,250,009-10,251,208 SNAP25
    nsv5873265copy number variation1nstd209human GRCh38 chr20: 10,285,558-10,287,326 , GRCh37.p13 chr20: 10,266,206-10,267,974 SNAP25
    nsv5726354mobile element insertion1nstd211human GRCh38 chr20: 10,245,441-10,245,441 , GRCh37.p13 chr20: 10,226,089-10,226,089 SNAP25
    nsv5726210mobile element insertion2nstd211human GRCh38 chr20: 10,285,676-10,285,676 , GRCh37.p13 chr20: 10,266,324-10,266,324 SNAP25
    nsv5665693insertion1nstd207human GRCh38 chr20: 10,224,772-10,224,772 , GRCh37.p13 chr20: 10,205,420-10,205,420 SNAP25
    nsv5602546copy number variation1nstd207human GRCh38 chr20: 10,233,460-10,233,788 , GRCh37.p13 chr20: 10,214,108-10,214,436 SNAP25
    nsv5561818mobile element insertion1nstd206human GRCh38 chr20: 10,285,676-10,285,727 , GRCh37.p13 chr20: 10,266,324-10,266,375 SNAP25
    nsv5531665copy number variation1nstd206human GRCh38 chr20: 10,233,258-10,233,401 , GRCh37.p13 chr20: 10,213,906-10,214,049 SNAP25
    nsv5531495copy number variation1nstd206human GRCh38 chr20: 10,233,462-10,233,789 , GRCh37.p13 chr20: 10,214,110-10,214,437 SNAP25
    nsv5531334copy number variation1nstd206human GRCh38 chr20: 10,265,110-10,272,846 , GRCh37.p13 chr20: 10,245,758-10,253,494 SNAP25
    nsv5531251copy number variation1nstd206human GRCh38 chr20: 10,241,426-10,241,608 , GRCh37.p13 chr20: 10,222,074-10,222,256 SNAP25
    nsv5526030copy number variation1nstd206human GRCh38 chr20: 10,235,838-10,236,088 , GRCh37.p13 chr20: 10,216,486-10,216,736 SNAP25
    nsv5516100copy number variation1nstd206human GRCh38 chr20: 10,304,946-10,305,012 , GRCh37.p13 chr20: 10,285,594-10,285,660 SNAP25
    nsv5360048translocation1nstd200human GRCh38 chr20: 10,304,339-10,304,339 , GRCh38 chr20: 10,304,452-10,304,452 , GRCh37.p13 chr20: 10,284,987-10,284,987 , GRCh37.p13 chr20: 10,285,100-10,285,100 SNAP25
    nsv5360047translocation1nstd200human GRCh38 chr20: 10,260,442-10,260,442 , GRCh38 chr20: 10,260,507-10,260,507 , GRCh37.p13 chr20: 10,241,090-10,241,090 , GRCh37.p13 chr20: 10,241,155-10,241,155 SNAP25
    nsv5327120copy number variation1nstd204human GRCh38.p13 chr20: 10,233,232-10,233,426 , GRCh37.p13 chr20: 10,213,880-10,214,074 SNAP25
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