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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv952072copy number variation1nstd73human GRCh38.p12 chr16: 89,032,193-89,201,992 , GRCh37 chr16: 89,098,601-89,268,400 CDH15, SLC22A31, 6 more genes

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