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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6117350mobile element insertion1nstd186human GRCh37 chr12: 109,887,640-109,887,640 , GRCh38.p12 chr12: 109,449,835-109,449,835 KCTD10
    nsv5976490insertion1nstd209human GRCh38 chr12: 109,449,831-109,449,831 , GRCh37.p13 chr12: 109,887,636-109,887,636 KCTD10
    nsv5706778mobile element insertion2nstd211human GRCh38 chr12: 109,449,845-109,449,845 , GRCh37.p13 chr12: 109,887,650-109,887,650 KCTD10
    nsv5705018mobile element insertion1nstd211human GRCh38 chr12: 109,463,810-109,463,810 , GRCh37.p13 chr12: 109,901,615-109,901,615 KCTD10
    nsv5659254insertion1nstd207human GRCh38 chr12: 109,449,831-109,449,831 , GRCh37.p13 chr12: 109,887,636-109,887,636 KCTD10
    nsv5420925mobile element insertion1nstd206human GRCh38 chr12: 109,449,835-109,449,835 , GRCh37.p13 chr12: 109,887,640-109,887,640 KCTD10
    nsv5415966mobile element insertion1nstd206human GRCh38 chr12: 109,463,810-109,463,861 , GRCh37.p13 chr12: 109,901,615-109,901,666 KCTD10
    nsv5315387copy number variation1nstd204human GRCh38.p13 chr12: 109,448,595-109,451,494 , GRCh37.p13 chr12: 109,886,400-109,889,299 MYO1H, KCTD10
    nsv5271460copy number variation1nstd204human GRCh38.p13 chr12: 109,446,901-109,451,550 , GRCh37.p13 chr12: 109,884,706-109,889,355 MYO1H, KCTD10
    nsv5138993mobile element insertion1nstd203human GRCh38 chr12: 109,463,797-109,463,810 , GRCh37.p13 chr12: 109,901,602-109,901,615 KCTD10
    nsv5136899mobile element insertion1nstd203human GRCh38 chr12: 109,449,838-109,449,845 , GRCh37.p13 chr12: 109,887,643-109,887,650 KCTD10
    nsv5134917mobile element insertion1nstd203human GRCh38 chr12: 109,449,832-109,449,845 , GRCh37.p13 chr12: 109,887,637-109,887,650 KCTD10
    nsv5134722mobile element insertion1nstd203human GRCh38 chr12: 109,449,837-109,449,841 , GRCh37.p13 chr12: 109,887,642-109,887,646 KCTD10
    nsv5133836mobile element insertion1nstd203human GRCh38 chr12: 109,449,836-109,449,845 , GRCh37.p13 chr12: 109,887,641-109,887,650 KCTD10
    nsv5131973mobile element insertion1nstd203human GRCh38 chr12: 109,449,834-109,449,845 , GRCh37.p13 chr12: 109,887,639-109,887,650 KCTD10
    nsv5129739mobile element insertion1nstd203human GRCh38 chr12: 109,449,831-109,449,845 , GRCh37.p13 chr12: 109,887,636-109,887,650 KCTD10
    nsv5129015mobile element insertion1nstd203human GRCh38 chr12: 109,449,833-109,449,845 , GRCh37.p13 chr12: 109,887,638-109,887,650 KCTD10
    nsv5120930mobile element insertion1nstd203human GRCh38 chr12: 109,449,835-109,449,845 , GRCh37.p13 chr12: 109,887,640-109,887,650 KCTD10
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv4995540copy number variation1nstd200human GRCh38 chr12: 109,472,435-109,473,258 , GRCh37.p13 chr12: 109,910,240-109,911,063 KCTD10
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