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Items: 5

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    Number of Variants: 5

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6622316copy number variation3nstd224human GRCh37 chr14: 46,474,288-46,560,423 , GRCh38.p12 chr14: 46,005,085-46,091,220 LINC00871
    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
    nsv6624930copy number variation25nstd224human GRCh37 chr19: 43,262,353-43,344,686 , GRCh38.p12 chr19: 42,758,201-42,840,534 CEACAMP6, PSG8-AS1, 2 more genes
    nsv6625871copy number variation20nstd224human GRCh37 chr1: 1,663,831-1,680,219 , GRCh38.p12 chr1: 1,732,392-1,748,780 LOC100129381, LOC112268218, 1 more genes
    nsv6621457copy number variation226nstd224human GRCh37 chr12: 31,266,287-31,406,907 , GRCh38.p12 chr12: 31,113,353-31,253,973 , GRCh38.p12 chr12|NT_187587.1: 1,874-144,767 OVOS2, RPL13AP22, 6 more genes
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