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Items: 5

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    Number of Variants: 5

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6630884copy number variation168nstd224human GRCh37 chr5: 814,876-825,329 , GRCh38.p12 chr5: 814,761-825,214 ZDHHC11, SPCS2P3
    nsv6620544copy number variation50nstd224human GRCh37 chr10: 45,218,841-45,359,483 , GRCh38.p12 chr10: 44,723,393-44,864,035 EIF2AP4, TMEM72-AS1
    nsv6620821copy number variation1nstd224human GRCh37 chr11: 134,395,242-134,715,777 , GRCh38.p12 chr11: 134,525,348-134,845,883 LINC02714, LOC105369583, 1 more genes
    nsv6622094copy number variation1nstd224human GRCh37 chr12: 93,134,648-93,251,098 , GRCh38.p12 chr12: 92,740,872-92,857,322 PLEKHG7, LOC100287544, 1 more genes
    nsv6628747copy number variation1nstd224human GRCh37 chr3: 193,444,413-193,618,979 , GRCh38.p12 chr3: 193,726,624-193,901,190 LOC105374282, LOC105374283, 5 more genes
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