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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115099mobile element insertion1nstd186human GRCh37 chr17: 76,052,946-76,052,997 , GRCh38.p12 chr17: 78,056,865-78,056,916 TNRC6C
    nsv5970391insertion1nstd209human GRCh38 chr17: 78,056,854-78,056,854 , GRCh37.p13 chr17: 76,052,935-76,052,935 TNRC6C
    nsv5969259insertion1nstd209human GRCh38 chr17: 77,985,601-77,985,601 , GRCh37.p13 chr17: 75,981,682-75,981,682 TNRC6C
    nsv5931262copy number variation1nstd209human GRCh38 chr17: 77,992,201-77,992,515 , GRCh37.p13 chr17: 75,988,282-75,988,596 TNRC6C
    nsv5713695mobile element insertion2nstd211human GRCh38 chr17: 78,056,865-78,056,865 , GRCh37.p13 chr17: 76,052,946-76,052,946 TNRC6C
    nsv5708402mobile element insertion1nstd211human GRCh38 chr17: 78,106,699-78,106,699 , GRCh37.p13 chr17: 76,102,780-76,102,780 TMC6, TNRC6C
    nsv5705795mobile element insertion1nstd211human GRCh38 chr17: 77,992,518-77,992,518 , GRCh37.p13 chr17: 75,988,599-75,988,599 TNRC6C
    nsv5699872mobile element insertion1nstd211human GRCh38 chr17: 77,992,525-77,992,525 , GRCh37.p13 chr17: 75,988,606-75,988,606 TNRC6C
    nsv5699319mobile element insertion1nstd211human GRCh38 chr17: 77,990,646-77,990,646 , GRCh37.p13 chr17: 75,986,727-75,986,727 TNRC6C
    nsv5696880mobile element insertion1nstd211human GRCh38 chr17: 78,070,440-78,070,440 , GRCh37.p13 chr17: 76,066,521-76,066,521 TNRC6C
    nsv5647853insertion1nstd207human GRCh38 chr17: 78,056,854-78,056,854 , GRCh37.p13 chr17: 76,052,935-76,052,935 TNRC6C
    nsv5589195copy number variation1nstd207human GRCh38 chr17: 77,992,201-77,992,515 , GRCh37.p13 chr17: 75,988,282-75,988,596 TNRC6C
    nsv5529355copy number variation1nstd206human GRCh38 chr17: 78,043,024-78,043,122 , GRCh37.p13 chr17: 76,039,105-76,039,203 TNRC6C
    nsv5525611copy number variation1nstd206human GRCh38 chr17: 77,974,986-77,978,064 , GRCh37.p13 chr17: 75,971,067-75,974,145 TNRC6C
    nsv5525513copy number variation1nstd206human GRCh38 chr17: 78,044,189-78,046,440 , GRCh37.p13 chr17: 76,040,270-76,042,521 TNRC6C
    nsv5515620copy number variation1nstd206human GRCh38 chr17: 77,992,217-77,992,516 , GRCh37.p13 chr17: 75,988,298-75,988,597 TNRC6C
    nsv5514570copy number variation1nstd206human GRCh38 chr17: 78,021,895-78,030,259 , GRCh37.p13 chr17: 76,017,976-76,026,340 TNRC6C
    nsv5433495mobile element insertion1nstd206human GRCh38 chr17: 77,990,646-77,990,697 , GRCh37.p13 chr17: 75,986,727-75,986,778 TNRC6C
    nsv5425209mobile element insertion1nstd206human GRCh38 chr17: 78,070,440-78,070,491 , GRCh37.p13 chr17: 76,066,521-76,066,572 TNRC6C
    nsv5416319mobile element insertion1nstd206human GRCh38 chr17: 78,056,865-78,056,916 , GRCh37.p13 chr17: 76,052,946-76,052,997 TNRC6C
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