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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv953959copy number variation1nstd73human GRCh37 chr19: 7,734,201-7,765,300 , GRCh38.p12 chr19: 7,669,315-7,700,414 FCER2, RETN, 2 more genes

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