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Items: 1 to 20 of 531

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958273insertion1nstd209human GRCh38 chr6: 99,550,659-99,550,659 , GRCh37.p13 chr6: 99,998,535-99,998,535 TSTD3, CCNC
    nsv5949095insertion1nstd209human GRCh38 chr6: 99,493,970-99,493,970 , GRCh37.p13 chr6: 99,941,846-99,941,846 USP45, TSTD3
    nsv5899494copy number variation1nstd209human GRCh38 chr6: 99,578,522-99,578,589 , GRCh37.p13 chr6: 100,026,398-100,026,465 TSTD3
    nsv5898819copy number variation1nstd209human GRCh38 chr6: 99,556,758-99,557,642 , GRCh37.p13 chr6: 100,004,634-100,005,518 TSTD3, CCNC
    nsv5729395mobile element insertion1nstd211human GRCh38 chr6: 99,481,479-99,481,479 , GRCh37.p13 chr6: 99,929,355-99,929,355 USP45, TSTD3
    nsv5691674mobile element insertion2nstd211human GRCh38 chr6: 99,550,671-99,550,671 , GRCh37.p13 chr6: 99,998,547-99,998,547 TSTD3, CCNC
    nsv5680395mobile element insertion1nstd211human GRCh38 chr6: 99,454,409-99,454,409 , GRCh37.p13 chr6: 99,902,285-99,902,285 TSTD3, USP45
    nsv5635558insertion1nstd207human GRCh38 chr6: 99,550,659-99,550,659 , GRCh37.p13 chr6: 99,998,535-99,998,535 CCNC, TSTD3
    nsv5626979insertion1nstd207human GRCh38 chr6: 99,478,511-99,478,511 , GRCh37.p13 chr6: 99,926,387-99,926,387 TSTD3, USP45
    nsv5542807insertion1nstd206human GRCh38 chr6: 99,462,428-99,462,428 , GRCh37.p13 chr6: 99,910,304-99,910,304 TSTD3, USP45
    nsv5534183insertion1nstd206human GRCh38 chr6: 99,490,697-99,490,705 , GRCh37.p13 chr6: 99,938,573-99,938,581 USP45, TSTD3
    nsv5465255copy number variation1nstd206human GRCh38 chr6: 99,477,088-99,477,668 , GRCh37.p13 chr6: 99,924,964-99,925,544 USP45, TSTD3
    nsv5463951copy number variation1nstd206human GRCh38 chr6: 99,519,468-99,524,678 , GRCh37.p13 chr6: 99,967,344-99,972,554 TSTD3
    nsv5457566copy number variation1nstd206human GRCh38 chr6: 99,477,627-99,477,883 , GRCh37.p13 chr6: 99,925,503-99,925,759 TSTD3, USP45
    nsv5455450copy number variation1nstd206human GRCh38 chr6: 99,467,208-99,469,814 , GRCh37.p13 chr6: 99,915,084-99,917,690 TSTD3, USP45
    nsv5454150copy number variation1nstd206human GRCh38 chr6: 99,578,523-99,578,590 , GRCh37.p13 chr6: 100,026,399-100,026,466 TSTD3
    nsv5404177mobile element insertion1nstd206human GRCh38 chr6: 99,454,409-99,454,460 , GRCh37.p13 chr6: 99,902,285-99,902,336 USP45, TSTD3
    nsv5393967mobile element insertion1nstd206human GRCh38 chr6: 99,550,671-99,550,722 , GRCh37.p13 chr6: 99,998,547-99,998,598 CCNC, TSTD3
    nsv5369521translocation1nstd200human GRCh38 chr6: 99,542,723-99,542,723 , GRCh38 chr6: 99,542,864-99,542,864 , GRCh37.p13 chr6: 99,990,599-99,990,599 , GRCh37.p13 chr6: 99,990,740-99,990,740 TSTD3, CCNC
    nsv5369520translocation1nstd200human GRCh38 chr6: 99,467,389-99,467,389 , GRCh38 chr6: 99,467,566-99,467,566 , GRCh37.p13 chr6: 99,915,442-99,915,442 , GRCh37.p13 chr6: 99,915,265-99,915,265 TSTD3, USP45
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