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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3587706copy number variation3estd214human GRCh37 chr1: 159,927,023-159,929,289 , GRCh38.p12 chr1: 159,957,233-159,959,499 SLAMF9, LINC01133

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