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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv997106copy number variation1nstd45humanPathogenic GRCh37 chrX: 22,050,562-22,269,427 , GRCh38.p12 chrX: 22,032,444-22,251,310 PHEX, PTCHD1-AS, 1 more genes

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