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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4411883copy number variation1nstd174human GRCh37 chr2: 174,797,106-174,801,099 , GRCh38.p12 chr2: 173,932,378-173,936,371 SP3
    esv3593395copy number variation6estd214human GRCh37 chr2: 174,796,967-174,801,225 , GRCh38.p12 chr2: 173,932,239-173,936,497 SP3

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