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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6289937copy number variation1nstd102humanPathogenic; other GRCh37 chr7: 100,769,707-100,769,707 , GRCh38 chr7: 101,126,426-101,126,426 SERPINE1

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