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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142643copy number variation1nstd232human GRCh38.p12 chr16: 30,892,747-30,892,838 , GRCh37.p13 chr16: 30,904,068-30,904,159 BCL7C, MIR762, 1 more genes
    nsv7094579copy number variation1nstd102humanUncertain significance GRCh37 chr16: 30,712,146-31,021,717 , GRCh38.p12 chr16: 30,700,825-31,010,396 FBXL19-AS1, BCL7C, 19 more genes
    nsv7068091inversion1nstd229human GRCh38 chr16: 29,736,414-31,610,190 , GRCh37.p13 chr16: 29,747,735-31,621,511 C16orf92, TMEM219, 118 more genes
    nsv7060598inversion1nstd229human GRCh38 chr16: 30,168,175-31,279,114 , GRCh37.p13 chr16: 30,179,496-31,290,435 ZNF629, ZNF771, 72 more genes
    nsv6997690copy number variation1nstd229human GRCh38 chr16: 30,876,378-30,889,877 , GRCh37.p13 chr16: 30,887,699-30,901,198 BCL7C, MIR762HG
    nsv6997610copy number variation1nstd229human GRCh38 chr16: 30,878,593-30,886,922 , GRCh37.p13 chr16: 30,889,914-30,898,243 BCL7C, MIR762HG
    nsv6995541copy number variation1nstd229human GRCh38 chr16: 30,769,801-30,859,400 , GRCh37.p13 chr16: 30,781,122-30,870,721 BCL7C, LOC647086, 2 more genes
    nsv6993341copy number variation1nstd229human GRCh38 chr16: 30,831,401-30,837,100 , GRCh37.p13 chr16: 30,842,722-30,848,421 BCL7C
    nsv6992677copy number variation1nstd229human GRCh38 chr16: 30,859,398-31,135,376 , GRCh37.p13 chr16: 30,870,719-31,146,697 SETD1A, HSD3B7, 19 more genes
    nsv6989265copy number variation1nstd229human GRCh38 chr16: 30,841,977-30,842,163 , GRCh37.p13 chr16: 30,853,298-30,853,484 BCL7C
    nsv6985576copy number variation1nstd229human GRCh38 chr16: 30,864,901-30,871,700 , GRCh37.p13 chr16: 30,876,222-30,883,021 BCL7C
    nsv6984899copy number variation1nstd229human GRCh38 chr16: 30,840,301-30,843,400 , GRCh37.p13 chr16: 30,851,622-30,854,721 BCL7C
    nsv6984651copy number variation1nstd229human GRCh38 chr16: 30,881,978-30,889,623 , GRCh37.p13 chr16: 30,893,299-30,900,944 BCL7C, MIR762HG
    nsv6980124copy number variation1nstd229human GRCh38 chr16: 30,830,000-30,836,169 , GRCh37.p13 chr16: 30,841,321-30,847,490 BCL7C
    nsv6637207copy number variation1nstd102humanUncertain significance GRCh37 chr16: 30,460,206-30,906,733 , GRCh38.p12 chr16: 30,448,885-30,895,412 ZNF629, ZNF689, 27 more genes
    nsv6590041inversion1nstd223human GRCh38 chr16: 29,736,419-31,610,189 , GRCh37.p13 chr16: 29,747,740-31,621,510 MIR762HG, FBXL19, 118 more genes
    nsv6586960inversion1nstd223human GRCh38 chr16: 30,855,180-30,855,975 , GRCh37.p13 chr16: 30,866,501-30,867,296 BCL7C
    nsv6514969copy number variation1nstd223human GRCh38 chr16: 30,838,778-30,846,059 , GRCh37.p13 chr16: 30,850,099-30,857,380 BCL7C
    nsv6513986copy number variation1nstd223human GRCh38 chr16: 30,883,501-30,884,800 , GRCh37.p13 chr16: 30,894,822-30,896,121 MIR762HG, BCL7C
    nsv6513552copy number variation1nstd223human GRCh38 chr16: 30,837,331-30,837,622 , GRCh37.p13 chr16: 30,848,652-30,848,943 BCL7C
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