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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4578340copy number variation2nstd181human GRCh37 chr2: 44,664,433-44,846,960 , GRCh38.p12 chr2: 44,437,294-44,619,821 CAMKMT

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