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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv829173copy number variation1nstd67human NCBI36 chr22: 29,780,043-29,873,956 , GRCh38.p12 chr22: 31,054,057-31,147,970 , GRCh37.p13 chr22: 31,450,043-31,543,956 SMTN, INPP5J, 5 more genes

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