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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv953941copy number variation1nstd73human GRCh37 chr19: 1,205,601-1,322,400 , GRCh38.p12 chr19: 1,205,602-1,322,401 STK11, FAM174C, 10 more genes

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