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Items: 1 to 20 of 290

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6117673copy number variation1nstd186human GRCh37 chr6: 31,948,777-32,013,177 , GRCh38.p12 chr6: 31,981,000-32,045,400 C4A, C4B, 6 more genes
    nsv5898146copy number variation1nstd209human GRCh38 chr6: 31,977,322-31,977,937 , GRCh37.p13 chr6: 31,945,099-31,945,714 STK19
    nsv5466552copy number variation1nstd206human GRCh38 chr6: 31,977,343-31,977,938 , GRCh37.p13 chr6: 31,945,120-31,945,715 STK19
    nsv5418497copy number variation1nstd206human GRCh38 chr6: 31,981,000-32,045,400 , GRCh37.p13 chr6: 31,948,777-32,013,177 C4A, C4B, 6 more genes
    nsv5362818translocation1nstd200human GRCh38 chr6: 31,977,938-31,977,938 , GRCh38 chr6: 31,977,343-31,977,343 , GRCh37.p13 chr6: 31,945,715-31,945,715 , GRCh37.p13 chr6: 31,945,120-31,945,120 STK19
    nsv5309885copy number variation1nstd204human GRCh38.p13 chr6: 31,977,319-31,977,959 , GRCh37.p13 chr6: 31,945,096-31,945,736 STK19
    nsv5235615copy number variation1nstd204human GRCh38.p13 chr6: 31,902,701-32,045,200 , GRCh37.p13 chr6: 31,870,478-32,012,977 STK19, ZBTB12, 14 more genes
    nsv5234584copy number variation1nstd204human GRCh38.p13 chr6: 31,976,901-31,994,500 , GRCh37.p13 chr6: 31,944,678-31,962,277 C4A, STK19
    nsv5234405copy number variation1nstd204human GRCh38.p13 chr6: 30,240,001-32,313,700 , GRCh37.p13 chr6: 30,207,778-32,281,477 DDAH2, LOC105375018, 175 more genes
    nsv5234261copy number variation1nstd204human GRCh38.p13 chr6: 31,980,001-31,984,700 , GRCh37.p13 chr6: 31,947,778-31,952,477 C4A, STK19
    nsv5233384copy number variation1nstd204human GRCh37.p13 chr6: 31,948,578-32,013,677 , GRCh38.p13 chr6: 31,980,801-32,045,900 C4A, C4B, 6 more genes
    nsv5230638copy number variation1nstd204human GRCh38.p13 chr6: 31,980,701-31,986,900 , GRCh37.p13 chr6: 31,948,478-31,954,677 C4A, STK19
    nsv5229879copy number variation1nstd204human GRCh38.p13 chr6: 31,502,001-32,151,900 , GRCh37.p13 chr6: 31,469,778-32,119,677 LTB, PPT2, 80 more genes
    nsv5113623mobile element insertion1nstd203human GRCh38 chr6: 31,978,163-31,978,173 , GRCh37.p13 chr6: 31,945,940-31,945,950 STK19
    nsv5105083mobile element insertion1nstd203human GRCh38 chr6: 31,978,157-31,978,173 , GRCh37.p13 chr6: 31,945,934-31,945,950 STK19
    nsv4815868copy number variation1nstd200human GRCh37 chr6: 31,945,120-31,945,715 , GRCh38.p12 chr6: 31,977,343-31,977,938 STK19
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4711380copy number variation1nstd195human GRCh37 chr6: 31,945,451-31,948,701 , GRCh38.p12 chr6: 31,977,674-31,980,924 C4A, STK19
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