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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112745copy number variation1nstd102humanPathogenic GRCh37 chr5: 176,812,675-176,813,587 , GRCh38.p12 chr5: 177,385,674-177,386,586 SLC34A1

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