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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967266insertion1nstd209human GRCh38 chr8: 132,200,387-132,200,387 , GRCh37.p13 chr8: 133,212,634-133,212,634 KCNQ3
    nsv5963873insertion1nstd209human GRCh38 chr8: 132,303,579-132,303,579 , GRCh37.p13 chr8: 133,315,826-133,315,826 KCNQ3
    nsv5949471insertion1nstd209human GRCh38 chr8: 132,154,193-132,154,193 , GRCh37.p13 chr8: 133,166,440-133,166,440 KCNQ3
    nsv5925586copy number variation1nstd209human GRCh38 chr8: 132,376,691-132,385,945 , GRCh37.p13 chr8: 133,388,938-133,398,192 KCNQ3
    nsv5919377copy number variation1nstd209human GRCh38 chr8: 132,187,764-132,187,937 , GRCh37.p13 chr8: 133,200,011-133,200,184 KCNQ3
    nsv5914858copy number variation1nstd209human GRCh38 chr8: 132,160,621-132,160,687 , GRCh37.p13 chr8: 133,172,868-133,172,934 KCNQ3
    nsv5913295copy number variation1nstd209human GRCh38 chr8: 132,164,243-132,164,420 , GRCh37.p13 chr8: 133,176,490-133,176,667 KCNQ3
    nsv5861923copy number variation1nstd209human GRCh38 chr8: 132,376,940-132,385,959 , GRCh37.p13 chr8: 133,389,187-133,398,206 KCNQ3
    nsv5856515copy number variation1nstd209human GRCh38 chr8: 132,383,910-132,385,309 , GRCh37.p13 chr8: 133,396,157-133,397,556 KCNQ3
    nsv5724695mobile element insertion1nstd211human GRCh38 chr8: 132,438,368-132,438,368 , GRCh37.p13 chr8: 133,450,615-133,450,615 KCNQ3
    nsv5720897mobile element insertion1nstd211human GRCh38 chr8: 132,333,390-132,333,390 , GRCh37.p13 chr8: 133,345,637-133,345,637 KCNQ3
    nsv5720640mobile element insertion1nstd211human GRCh38 chr8: 132,131,037-132,131,037 , GRCh37.p13 chr8: 133,143,284-133,143,284 KCNQ3
    nsv5719464mobile element insertion1nstd211human GRCh38 chr8: 132,297,717-132,297,717 , GRCh37.p13 chr8: 133,309,964-133,309,964 KCNQ3
    nsv5711512mobile element insertion1nstd211human GRCh38 chr8: 132,467,253-132,467,253 , GRCh37.p13 chr8: 133,479,500-133,479,500 KCNQ3
    nsv5705561mobile element insertion2nstd211human GRCh38 chr8: 132,128,607-132,128,607 , GRCh37.p13 chr8: 133,140,854-133,140,854 KCNQ3
    nsv5702098mobile element insertion1nstd211human GRCh38 chr8: 132,425,562-132,425,562 , GRCh37.p13 chr8: 133,437,809-133,437,809 KCNQ3
    nsv5674053copy number variation1nstd102humanPathogenic GRCh37 chr8: 133,141,509-133,492,779 , GRCh38.p12 chr8: 132,129,262-132,480,532 KCNQ3
    nsv5673945copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr8: 133,141,509-134,296,554 , GRCh38.p12 chr8: 132,129,262-133,284,311 SLA, TMEM71, 15 more genes
    nsv5643609insertion1nstd207human GRCh38 chr8: 132,146,780-132,146,780 , GRCh37.p13 chr8: 133,159,027-133,159,027 KCNQ3
    nsv5642813insertion1nstd207human GRCh38 chr8: 132,303,565-132,303,565 , GRCh37.p13 chr8: 133,315,812-133,315,812 KCNQ3
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