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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6289954copy number variation1nstd102humanPathogenic GRCh37 chr16: 68,345,747-68,361,056 , GRCh38.p12 chr16: 68,311,844-68,327,153 PRMT7

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