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Items: 5

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    Number of Variants: 5

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6621719copy number variation1nstd224human GRCh37 chr12: 55,034,908-55,159,539 , GRCh38.p12 chr12: 54,641,124-54,765,755 DCD
    nsv6628174copy number variation4nstd224human GRCh37 chr2: 89,918,400-90,199,081 , GRCh38.p12 chr2: 89,879,590-90,160,226 IGKV6D-21, IGKV3D-25, 26 more genes
    nsv6620771copy number variation5nstd224human GRCh37 chr10: 85,154,286-85,213,365 , GRCh38.p12 chr10: 83,394,530-83,453,609 0
    nsv6628864copy number variation24nstd224human GRCh37 chr3: 65,193,246-65,221,937 , GRCh38.p12 chr3: 65,207,571-65,236,262 0
    nsv6626284copy number variation61nstd224human GRCh37 chr1: 752,566-846,808 , GRCh38.p12 chr1: 817,186-911,428 LINC00115, FAM41C, 5 more genes
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