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Items: 5

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    Number of Variants: 5

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6620491copy number variation1nstd224human GRCh37 chr10: 53,608,977-53,657,085 , GRCh38.p12 chr10: 51,849,217-51,897,325 PRKG1
    nsv6624465copy number variation1nstd224human GRCh37 chr19: 37,797,578-37,894,468 , GRCh38.p12 chr19: 37,306,676-37,403,566 ZNF527, ZNF875
    nsv6625910copy number variation1nstd224human GRCh37 chr1: 164,149,433-164,360,749 , GRCh38.p12 chr1: 164,180,196-164,391,512 HMGB3P6, RNU5F-6P, 1 more genes
    nsv6625130copy number variation188nstd224human GRCh37 chr19: 43,344,686-43,528,980 , GRCh38.p12 chr19: 42,840,534-43,024,828 CEACAMP7, PSG1, 4 more genes
    nsv6626470copy number variation13nstd224human GRCh37 chr1: 752,566-838,555 , GRCh38.p12 chr1: 817,186-903,175 LINC00115, FAM41C, 5 more genes
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