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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148067copy number variation1nstd102humanPathogenic GRCh38 chr16: 30,362-48,162 , GRCh37.p13 chr16: 80,362-98,162 IL9RP3, POLR3K

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