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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4423978copy number variation1nstd174human GRCh37 chr9: 114,165,061-114,170,342 , GRCh38.p12 chr9: 111,402,781-111,408,062 ECPAS
    esv3621488copy number variation440estd214human GRCh37 chr9: 114,165,663-114,169,729 , GRCh38.p12 chr9: 111,403,383-111,407,449 ECPAS

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