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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4634377copy number variation1nstd184human GRCh37 chrX: 149,613,840-150,156,259 , GRCh38.p12 chrX: 150,445,574-150,987,786 HMGB3, MTM1, 6 more genes

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