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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv435755copy number variation1nstd16human GRCh37.p13 chr3: 191,936,282-191,990,710 , GRCh38.p12 chr3: 192,218,493-192,272,921 , NCBI36 chr3: 193,418,976-193,473,404 FGF12, FGF12-AS1

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