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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5059940copy number variation1nstd202human GRCh37.p13 chr3|NW_003871058.1: 1-21,371 , GRCh37.p13 chr3: 60,558,332-60,579,702 , GRCh38 chr3: 60,569,163-60,593,969 FHIT

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