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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv833712copy number variation7nstd68human NCBI35 chr19: 3,181,780-3,316,288 , GRCh37.p13 chr19: 3,230,780-3,365,288 , GRCh38.p12 chr19: 3,230,782-3,365,290 NFIC, CELF5, 1 more genes

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