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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv438199copy number variation14nstd20human NCBI34 chr12: 27,539,977-27,545,038 , GRCh38.p12 chr12: 27,495,777-27,500,838 , GRCh37.p13 chr12: 27,648,710-27,653,771 SMCO2, RARS1P1

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