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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4422519copy number variation1nstd174human GRCh37 chr21: 43,225,946-43,226,565 , GRCh38.p12 chr21: 41,805,786-41,806,405 PRDM15
    esv2668746copy number variation247estd199human GRCh37 chr21: 43,226,213-43,226,565 , GRCh38.p12 chr21: 41,806,053-41,806,405 PRDM15

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