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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4684188copy number variation1nstd102humanPathogenic GRCh37 chr19: 33,792,329-33,792,330 , GRCh38 chr19: 33,301,423-33,301,424 CEBPA, CEBPA-DT
    nsv4578541copy number variation1nstd102humanPathogenic GRCh37 chr19: 33,792,369-33,792,370 , GRCh38 chr19: 33,301,463-33,301,464 CEBPA, CEBPA-DT

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