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Items: 7

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    Number of Variants: 7

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6628914copy number variation179nstd224human GRCh37 chr3: 173,259,356-173,289,281 , GRCh38.p12 chr3: 173,541,566-173,571,491 NLGN1
    nsv6620630copy number variation63nstd224human GRCh37 chr10: 47,543,322-47,646,751 , GRCh38.p12 chr10: 46,172,086-46,275,515 ANTXRLP1, AHCYP1
    nsv6628664copy number variation11nstd224human GRCh37 chr3: 161,883,401-161,956,676 , GRCh38.p12 chr3: 162,165,613-162,238,888 LOC107986049, LOC107986048
    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
    nsv6621087copy number variation1nstd224human GRCh37 chr11: 381,754-408,352 , GRCh38.p12 chr11: 381,754-408,352 PKP3, SIGIRR, 1 more genes
    nsv6621849copy number variation162nstd224human GRCh37 chr12: 8,003,758-8,123,306 , GRCh38.p12 chr12: 7,851,162-7,970,710 SLC2A14, RPS20P29, 3 more genes
    nsv6627726copy number variation214nstd224human GRCh37 chr2: 179,300,979-179,315,726 , GRCh38.p12 chr2: 178,436,252-178,450,999 PRKRA, PJVK, 1 more genes
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