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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv952384copy number variation1nstd73human GRCh37 chr17: 78,318,701-78,330,200 , GRCh38.p12 chr17: 80,344,901-80,356,400 RNF213, RNF213-AS1

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