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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4412281copy number variation1nstd174human GRCh37 chr2: 47,653,672-47,654,599 , GRCh38.p12 chr2: 47,426,533-47,427,460 MSH2
    esv2720024copy number variation76estd201human GRCh37 chr2: 47,653,672-47,654,462 , GRCh38.p12 chr2: 47,426,533-47,427,323 MSH2

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