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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4418327copy number variation1nstd174human GRCh37 chr22: 50,301,967-50,302,537 , GRCh38.p12 chr22: 49,908,319-49,908,889 ALG12
    esv2724721copy number variation3estd201human GRCh37 chr22: 50,301,982-50,302,537 , GRCh38.p12 chr22: 49,908,334-49,908,889 ALG12

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