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Items: 1 to 20 of 3332

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3919031copy number variation1nstd102humanPathogenic NCBI36 chr15: 91,307,893-91,375,475 , GRCh37 chr15: 93,506,889-93,574,471 , GRCh38 chr15: 92,963,659-93,031,241 CHD2
    nsv4681731copy number variation1nstd102humanPathogenic GRCh37 chr15: 93,510,535-93,555,694 , GRCh38.p12 chr15: 92,967,305-93,012,464 CHD2
    nsv7094644copy number variation1nstd102humanPathogenic GRCh37 chr15: 93,485,032-93,515,667 , GRCh38.p12 chr15: 92,941,802-92,972,437 CHD2
    nsv3888171copy number variation1nstd102humanPathogenic GRCh38 chr15: 92,996,937-93,014,929 , GRCh37 chr15: 93,540,167-93,558,159 CHD2
    nsv4682284copy number variation1nstd102humanPathogenic GRCh37 chr15: 93,482,788-93,487,765 , GRCh38.p12 chr15: 92,939,558-92,944,535 CHD2
    nsv5672831copy number variation1nstd102humanPathogenic GRCh37 chr15: 93,514,985-93,518,190 , GRCh38.p12 chr15: 92,971,755-92,974,960 CHD2
    nsv6309644copy number variation1nstd102humanPathogenic GRCh37 chr15: 93,521,444-93,522,533 , GRCh38.p12 chr15: 92,978,214-92,979,303 CHD2
    nsv6309814copy number variation1nstd102humanPathogenic GRCh37 chr15: 93,489,031-93,489,466 , GRCh38.p12 chr15: 92,945,801-92,946,236 CHD2
    nsv7094747copy number variation1nstd102humanPathogenic GRCh37 chr15: 93,528,708-93,528,923 , GRCh38.p12 chr15: 92,985,478-92,985,693 CHD2
    nsv4682719copy number variation1nstd102humanPathogenic GRCh37 chr15: 93,472,240-93,472,341 , GRCh38.p12 chr15: 92,929,010-92,929,111 CHD2
    nsv4682678copy number variation1nstd102humanPathogenic GRCh37 chr15: 93,444,448-93,444,549 , GRCh38.p12 chr15: 92,901,218-92,901,319 CHD2
    nsv7093309copy number variation1nstd102humanPathogenic GRCh37 chr15: 93,498,735-93,498,788 , GRCh38 chr15: 92,955,505-92,955,558 CHD2
    nsv5674324delins1nstd102humanPathogenic GRCh37 chr15: 93,540,229-93,540,235 , GRCh38 chr15: 92,996,999-92,997,005 CHD2
    nsv7094549copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 93,547,827-93,558,159 , GRCh38.p12 chr15: 93,004,597-93,014,929 CHD2
    nsv3902195copy number variation1nstd102humanBenign GRCh37 chr21: 41,521,231-41,521,681 , GRCh38.p12 chr21: 40,149,304-40,149,754 DSCAM
    nsv6634539copy number variation1nstd102humanBenign GRCh38 chr15: 92,972,558-92,972,870 , GRCh37 chr15: 93,515,788-93,516,100 CHD2
    esv4007319copy number variation1estd231human GRCh37 chr21: 41,586,865-41,587,190 , GRCh38.p12 chr21: 40,214,938-40,215,263 DSCAM
    esv4006214copy number variation1estd231human GRCh37 chr15: 93,515,787-93,516,100 , GRCh38.p12 chr15: 92,972,557-92,972,870 CHD2
    nsv6309815copy number variation1nstd102humanUncertain significance GRCh37 chr15: 93,510,535-93,567,935 , GRCh38.p12 chr15: 92,967,305-93,024,705 CHD2
    nsv3918709copy number variation1nstd102humanUncertain significance NCBI36 chr15: 91,321,456-91,374,888 , GRCh37.p13 chr15: 93,520,452-93,573,884 , GRCh38.p12 chr15: 92,977,222-93,030,654 CHD2
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