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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv509301insertion1nstd49human GRCh38.p12 chr9: 34,703,177-34,799,269 , NCBI35 chr9: 34,693,174-34,789,266 , GRCh37.p13 chr9: 34,703,174-34,799,266 CCL21, SPATA31F1

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