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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3971772copy number variation1nstd102humanPathogenic GRCh38 chr12: 53,306,793-53,321,761 , GRCh37.p13 chr12: 53,700,577-53,715,545 MYG1, AAAS

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