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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv831666copy number variation2nstd68human NCBI35 chr9: 98,954,540-99,098,245 , GRCh37.p13 chr9: 101,874,985-102,018,690 , GRCh38.p12 chr9: 99,112,703-99,256,408 TGFBR1, SEC61B, 4 more genes

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