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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6309359copy number variation1nstd102humanPathogenic GRCh37 chr14: 73,673,074-73,673,200 , GRCh38.p12 chr14: 73,206,366-73,206,492 PSEN1

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