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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4417822copy number variation1nstd174human GRCh37 chr12: 124,824,096-124,824,358 , GRCh38.p12 chr12: 124,339,550-124,339,812 NCOR2
    esv2666569copy number variation119estd199human GRCh37 chr12: 124,824,145-124,824,277 , GRCh38.p12 chr12: 124,339,599-124,339,731 NCOR2

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