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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3568437copy number variation11estd212human GRCh37 chr22: 45,130,466-45,137,204 , GRCh38.p12 chr22: 44,734,586-44,741,324 PRR5-ARHGAP8, PRR5

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