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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4683382copy number variation1nstd102humanUncertain significance GRCh37 chr11: 19,206,489-19,209,861 , GRCh38.p12 chr11: 19,184,942-19,188,314 CSRP3

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