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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3580574copy number variation2estd212human GRCh37 chr13: 24,148,280-24,156,765 , GRCh38.p12 chr13: 23,574,141-23,582,626 TNFRSF19

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