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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6315329copy number variation1nstd102humanPathogenic GRCh38 chrX: 38,317,307-38,317,363 , GRCh37 chrX: 38,176,560-38,176,616 RPGR

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