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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1067925copy number variation328nstd104human GRCh37 chrY: 2,694,521-59,034,049 , GRCh38.p12 chrY: 2,826,480-56,887,902 ACTG1P2, AMELY, 525 more genes

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