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Items: 5

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    Number of Variants: 5

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6624844copy number variation645nstd224human GRCh37 chr19: 20,630,360-20,715,228 , GRCh38.p12 chr19: 20,447,554-20,532,422 ZNF737, LOC105372316, 1 more genes
    nsv6634059copy number variation43nstd224human GRCh37 chrX: 47,911,871-47,970,727 , GRCh38.p12 chrX: 48,052,481-48,111,343 SSX6P, ZNF630, 1 more genes
    nsv6620867copy number variation1nstd224human GRCh37 chr11: 100,276,633-100,390,879 , GRCh38.p12 chr11: 100,405,902-100,520,148 0
    nsv6632516copy number variation3nstd224human GRCh37 chr8: 15,699,845-15,716,896 , GRCh38.p12 chr8: 15,842,336-15,859,387 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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