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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4397214copy number variation1nstd174human GRCh37 chr3: 1,034,997-1,039,699 , GRCh38.p12 chr3: 993,313-998,015 CNTN6
    nsv514130copy number variation25nstd46human GRCh37.p13 chr3: 1,035,204-1,039,092 , GRCh38.p12 chr3: 993,520-997,408 , NCBI36 chr3: 1,010,204-1,014,092 CNTN6

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