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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5673427copy number variation1nstd102humanPathogenic GRCh37 chr22: 29,083,885-30,337,586 , GRCh38.p12 chr22: 28,687,897-29,941,597 SNORD125, RASL10A, 36 more genes
    nsv5673351copy number variation1nstd102humanPathogenic GRCh37 chr22: 29,105,984-30,337,586 , GRCh38.p12 chr22: 28,709,996-29,941,597 SNORD125, RASL10A, 36 more genes
    nsv5673347copy number variation1nstd102humanPathogenic GRCh37 chr22: 29,082,731-29,138,822 , GRCh38.p12 chr22: 28,686,743-28,742,834 HSCB, CHEK2
    nsv5552004copy number variation1nstd206human GRCh38 chr22: 28,745,258-28,747,976 , GRCh37.p13 chr22: 29,141,246-29,143,964 HSCB
    nsv5549177copy number variation1nstd206human GRCh38 chr22: 28,752,497-28,752,872 , GRCh37.p13 chr22: 29,148,485-29,148,860 HSCB
    nsv5546974copy number variation1nstd206human GRCh38 chr22: 28,747,651-28,767,952 , GRCh37.p13 chr22: 29,143,639-29,163,940 HSCB
    nsv5544737copy number variation1nstd206human GRCh38 chr22: 28,751,620-28,752,608 , GRCh37.p13 chr22: 29,147,608-29,148,596 HSCB
    nsv5538945copy number variation1nstd206human GRCh38 chr22: 28,752,253-28,753,360 , GRCh37.p13 chr22: 29,148,241-29,149,348 HSCB
    nsv5322609copy number variation1nstd204human GRCh38.p13 chr22: 28,715,195-28,751,334 , GRCh37.p13 chr22: 29,111,183-29,147,322 CHEK2, HSCB
    nsv5295776copy number variation1nstd204human GRCh38.p13 chr22: 28,723,601-28,751,300 , GRCh37.p13 chr22: 29,119,589-29,147,288 HSCB, CHEK2
    nsv5289251copy number variation1nstd204human GRCh38.p13 chr22: 28,685,201-28,779,600 , GRCh37.p13 chr22: 29,081,189-29,175,588 HSCB, CHEK2, 1 more genes
    nsv5287345copy number variation1nstd204human GRCh38.p13 chr22: 28,720,907-28,748,906 , GRCh37.p13 chr22: 29,116,895-29,144,894 HSCB, CHEK2
    nsv5168422mobile element insertion1nstd203human GRCh38 chr22: 28,745,341-28,745,368 , GRCh37.p13 chr22: 29,141,329-29,141,356 HSCB
    nsv5166141mobile element insertion1nstd203human GRCh38 chr22: 28,750,945-28,750,969 , GRCh37.p13 chr22: 29,146,933-29,146,957 HSCB
    nsv5041306copy number variation1nstd200human GRCh38 chr22: 28,739,515-28,753,944 , GRCh37.p13 chr22: 29,135,503-29,149,932 HSCB, CHEK2
    nsv5035829copy number variation1nstd200human GRCh38 chr22: 28,754,759-28,763,841 , GRCh37.p13 chr22: 29,150,747-29,159,829 HSCB
    nsv5034985copy number variation1nstd200human GRCh38 chr22: 28,752,793-28,752,927 , GRCh37.p13 chr22: 29,148,781-29,148,915 HSCB
    nsv5032177copy number variation1nstd200human GRCh38 chr22: 28,753,606-28,756,033 , GRCh37.p13 chr22: 29,149,594-29,152,021 HSCB
    nsv5030799copy number variation1nstd200human GRCh38 chr22: 28,753,590-28,755,154 , GRCh37.p13 chr22: 29,149,578-29,151,142 HSCB
    nsv4869394copy number variation1nstd200human GRCh37 chr22: 29,150,747-29,159,829 , GRCh38.p12 chr22: 28,754,759-28,763,841 HSCB
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