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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv508200copy number variation3nstd49human GRCh38.p12 chr2: 219,134,744-219,202,175 , NCBI35 chr2: 219,824,971-219,892,402 , GRCh37.p13 chr2: 219,999,466-220,066,897 CNPPD1, RETREG2, 2 more genes

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