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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4681970copy number variation1nstd102humanPathogenic GRCh37 chr7: 73,482,967-73,483,050 , GRCh38.p12 chr7: 74,068,637-74,068,720 ELN

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