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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1066496copy number variation1nstd100human NCBI36 chr22: 49,006,739-49,073,001 , GRCh37.p13 chr22: 50,664,612-50,730,874 , GRCh38.p12 chr22: 50,226,183-50,292,445 MAPK11, PLXNB2, 3 more genes

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