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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923186copy number variation1nstd209human GRCh38 chr7: 12,242,077-12,242,398 , GRCh37.p13 chr7: 12,281,703-12,282,024 TMEM106B
    nsv5918832copy number variation1nstd209human GRCh38 chr7: 12,229,520-12,229,594 , GRCh37.p13 chr7: 12,269,146-12,269,220 TMEM106B
    nsv5730168mobile element insertion1nstd211human GRCh38 chr7: 12,243,134-12,243,134 , GRCh37.p13 chr7: 12,282,760-12,282,760 TMEM106B
    nsv5691744mobile element insertion1nstd211human GRCh38 chr7: 12,234,194-12,234,194 , GRCh37.p13 chr7: 12,273,820-12,273,820 TMEM106B
    nsv5580225copy number variation1nstd207human GRCh38 chr7: 12,242,077-12,242,398 , GRCh37.p13 chr7: 12,281,703-12,282,024 TMEM106B
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5534743insertion1nstd206human GRCh38 chr7: 12,219,669-12,219,676 , GRCh37.p13 chr7: 12,259,295-12,259,302 TMEM106B
    nsv5469184copy number variation1nstd206human GRCh38 chr7: 12,211,863-12,260,489 , GRCh37.p13 chr7: 12,251,489-12,300,115 TMEM106B
    nsv5467984copy number variation1nstd206human GRCh38 chr7: 12,237,692-12,244,534 , GRCh37.p13 chr7: 12,277,318-12,284,160 TMEM106B
    nsv5465862copy number variation1nstd206human GRCh38 chr7: 12,242,085-12,242,399 , GRCh37.p13 chr7: 12,281,711-12,282,025 TMEM106B
    nsv5464969copy number variation1nstd206human GRCh38 chr7: 12,198,143-12,246,727 , GRCh37.p13 chr7: 12,237,769-12,286,353 TMEM106B
    nsv5411302mobile element insertion1nstd206human GRCh38 chr7: 12,234,194-12,234,245 , GRCh37.p13 chr7: 12,273,820-12,273,871 TMEM106B
    nsv5383082mobile element deletion2nstd186human GRCh37 chr7: 12,281,711-12,282,025 , GRCh38.p12 chr7: 12,242,085-12,242,399 TMEM106B
    nsv5370259translocation1nstd200human GRCh38 chr7: 12,243,261-12,243,261 , GRCh38 chr7: 12,243,318-12,243,318 , GRCh37.p13 chr7: 12,282,887-12,282,887 , GRCh37.p13 chr7: 12,282,944-12,282,944 TMEM106B
    nsv5239273copy number variation1nstd204human GRCh38.p13 chr7: 12,230,801-12,236,800 , GRCh37.p13 chr7: 12,270,427-12,276,426 TMEM106B
    nsv5233755copy number variation1nstd204human GRCh38.p13 chr7: 12,242,101-12,242,400 , GRCh37.p13 chr7: 12,281,727-12,282,026 TMEM106B
    nsv5216288mobile element deletion1nstd204human GRCh38.p13 chr7: 12,242,085-12,242,399 , GRCh37.p13 chr7: 12,281,711-12,282,025 TMEM106B
    nsv5118615mobile element insertion1nstd203human GRCh38 chr7: 12,224,809-12,224,825 , GRCh37.p13 chr7: 12,264,435-12,264,451 TMEM106B
    nsv4955432copy number variation1nstd200human GRCh38 chr7: 12,214,216-12,214,336 , GRCh37.p13 chr7: 12,253,842-12,253,962 TMEM106B
    nsv4955431copy number variation1nstd200human GRCh38 chr7: 12,212,612-12,214,065 , GRCh37.p13 chr7: 12,252,238-12,253,691 TMEM106B
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