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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6315303copy number variation1nstd102humanPathogenic GRCh37 chr1: 150,485,082-150,486,244 , GRCh38 chr1: 150,512,606-150,513,768 FALEC, ECM1

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