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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4406950copy number variation1nstd174human GRCh37 chr1: 152,327,395-152,327,727 , GRCh38.p12 chr1: 152,354,919-152,355,251 FLG-AS1, FLG2
    esv2663079copy number variation128estd199human GRCh37 chr1: 152,327,436-152,327,667 , GRCh38.p12 chr1: 152,354,960-152,355,191 FLG-AS1, FLG2

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