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Items: 1 to 20 of 272

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950945insertion1nstd209human GRCh38 chr6: 44,044,803-44,044,803 , GRCh37.p13 chr6: 44,012,540-44,012,540 SCIRT
    nsv5688580mobile element insertion2nstd211human GRCh38 chr6: 44,061,233-44,061,233 , GRCh37.p13 chr6: 44,028,970-44,028,970 SCIRT
    nsv5643760insertion1nstd207human GRCh38 chr6: 44,042,411-44,042,411 , GRCh37.p13 chr6: 44,010,148-44,010,148 SCIRT
    nsv5636113insertion1nstd207human GRCh38 chr6: 44,044,815-44,044,815 , GRCh37.p13 chr6: 44,012,552-44,012,552 SCIRT
    nsv5568358copy number variation1nstd207human GRCh38 chr6: 44,066,584-44,066,736 , GRCh37.p13 chr6: 44,034,321-44,034,473 SCIRT
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5539876insertion1nstd206human GRCh38 chr6: 44,045,300-44,045,311 , GRCh37.p13 chr6: 44,013,037-44,013,048 SCIRT
    nsv5470241copy number variation1nstd206human GRCh38 chr6: 44,005,044-44,005,118 , GRCh37.p13 chr6: 43,972,781-43,972,855 SCIRT, LINC03040
    nsv5466639copy number variation1nstd206human GRCh38 chr6: 44,044,675-44,045,276 , GRCh37.p13 chr6: 44,012,412-44,013,013 SCIRT
    nsv5465717copy number variation1nstd206human GRCh38 chr6: 44,066,697-44,066,940 , GRCh37.p13 chr6: 44,034,434-44,034,677 SCIRT
    nsv5413210mobile element insertion1nstd206human GRCh38 chr6: 44,061,233-44,061,284 , GRCh37.p13 chr6: 44,028,970-44,029,021 SCIRT
    nsv5378437translocation1nstd200human GRCh38 chr6: 44,045,275-44,045,275 , GRCh38 chr6: 44,044,488-44,044,488 , GRCh37.p13 chr6: 44,013,012-44,013,012 , GRCh37.p13 chr6: 44,012,225-44,012,225 SCIRT
    nsv5378436translocation1nstd200human GRCh38 chr6: 44,020,542-44,020,542 , GRCh38 chr6: 44,022,712-44,022,712 , GRCh37.p13 chr6: 43,988,279-43,988,279 , GRCh37.p13 chr6: 43,990,449-43,990,449 SCIRT
    nsv5378435translocation1nstd200human GRCh38 chr6: 44,022,712-44,022,712 , GRCh38 chr6: 44,020,422-44,020,422 , GRCh37.p13 chr6: 43,990,449-43,990,449 , GRCh37.p13 chr6: 43,988,159-43,988,159 SCIRT
    nsv5362906translocation1nstd200human GRCh38 chr6: 44,020,079-44,020,079 , GRCh38 chr6: 44,020,171-44,020,171 , GRCh37.p13 chr6: 43,987,816-43,987,816 , GRCh37.p13 chr6: 43,987,908-43,987,908 SCIRT
    nsv5340647translocation1nstd200human GRCh37 chr6: 43,990,449-43,990,449 , GRCh37 chr6: 43,988,159-43,988,159 , GRCh38.p12 chr6: 44,022,712-44,022,712 , GRCh38.p12 chr6: 44,020,422-44,020,422 SCIRT
    nsv5340490translocation1nstd200human GRCh37 chr6: 43,990,449-43,990,449 , GRCh37 chr6: 43,988,279-43,988,279 , GRCh38.p12 chr6: 44,020,542-44,020,542 , GRCh38.p12 chr6: 44,022,712-44,022,712 SCIRT
    nsv5329991translocation1nstd200human GRCh37 chr6: 44,013,012-44,013,012 , GRCh37 chr6: 44,012,225-44,012,225 , GRCh38.p12 chr6: 44,045,275-44,045,275 , GRCh38.p12 chr6: 44,044,488-44,044,488 SCIRT
    nsv5322360translocation1nstd204human GRCh38.p13 chr6: 44,044,544-44,044,544 , GRCh38.p13 chr6: 44,045,276-44,045,276 , GRCh37.p13 chr6: 44,013,013-44,013,013 , GRCh37.p13 chr6: 44,012,281-44,012,281 SCIRT
    nsv5116064mobile element insertion1nstd203human GRCh38 chr6: 44,047,079-44,047,088 , GRCh37.p13 chr6: 44,014,816-44,014,825 SCIRT
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