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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1146118copy number variation1nstd107human GRCh37 chr22: 18,141,695-18,144,631 , GRCh38.p12 chr22: 17,658,929-17,661,865 BCL2L13

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