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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5932045copy number variation1nstd209human GRCh38 chr16: 48,588,246-48,592,482 , GRCh37.p13 chr16: 48,622,157-48,626,393 N4BP1
    nsv5930558copy number variation1nstd209human GRCh38 chr16: 48,604,548-48,604,645 , GRCh37.p13 chr16: 48,638,459-48,638,556 N4BP1
    nsv5928898copy number variation1nstd209human GRCh38 chr16: 48,586,610-48,597,683 , GRCh37.p13 chr16: 48,620,521-48,631,594 N4BP1
    nsv5871936copy number variation1nstd209human GRCh38 chr16: 48,591,757-48,597,656 , GRCh37.p13 chr16: 48,625,668-48,631,567 N4BP1
    nsv5869580copy number variation2nstd209human GRCh38 chr16: 48,596,807-48,597,806 , GRCh37.p13 chr16: 48,630,718-48,631,717 N4BP1
    nsv5869441copy number variation1nstd209human GRCh38 chr16: 48,587,457-48,592,556 , GRCh37.p13 chr16: 48,621,368-48,626,467 N4BP1
    nsv5588562copy number variation1nstd207human GRCh38 chr16: 48,604,548-48,604,645 , GRCh37.p13 chr16: 48,638,459-48,638,556 N4BP1
    nsv5528392copy number variation1nstd206human GRCh38 chr16: 48,598,721-48,598,798 , GRCh37.p13 chr16: 48,632,632-48,632,709 LOC105371239, N4BP1
    nsv5524021copy number variation1nstd206human GRCh38 chr16: 48,604,561-48,604,646 , GRCh37.p13 chr16: 48,638,472-48,638,557 N4BP1
    nsv5519022copy number variation1nstd206human GRCh38 chr16: 48,588,246-48,592,483 , GRCh37.p13 chr16: 48,622,157-48,626,394 N4BP1
    nsv5358157translocation1nstd200human GRCh38 chr16: 48,604,561-48,604,561 , GRCh38 chr16: 48,604,646-48,604,646 , GRCh37.p13 chr16: 48,638,472-48,638,472 , GRCh37.p13 chr16: 48,638,557-48,638,557 N4BP1
    nsv5004022copy number variation1nstd200human GRCh38 chr16: 48,604,128-48,605,209 , GRCh37.p13 chr16: 48,638,039-48,639,120 N4BP1
    nsv5004021copy number variation1nstd200human GRCh38 chr16: 48,598,721-48,598,798 , GRCh37.p13 chr16: 48,632,632-48,632,709 LOC105371239, N4BP1
    nsv5004020copy number variation1nstd200human GRCh38 chr16: 48,588,246-48,592,483 , GRCh37.p13 chr16: 48,622,157-48,626,394 N4BP1
    nsv5004019copy number variation1nstd200human GRCh38 chr16: 48,539,668-48,540,172 , GRCh37.p13 chr16: 48,573,579-48,574,083 , N4BP1
    nsv4857027copy number variation1nstd200human GRCh37 chr16: 48,623,456-48,623,919 , GRCh38.p12 chr16: 48,589,545-48,590,008 N4BP1
    nsv4857026copy number variation1nstd200human GRCh37 chr16: 48,622,157-48,626,394 , GRCh38.p12 chr16: 48,588,246-48,592,483 N4BP1
    nsv4857025copy number variation1nstd200human GRCh37 chr16: 48,620,524-48,631,595 , GRCh38.p12 chr16: 48,586,613-48,597,684 N4BP1
    nsv4857024copy number variation1nstd200human GRCh37 chr16: 48,573,579-48,574,083 , GRCh38.p12 chr16: 48,539,668-48,540,172 , N4BP1
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