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Items: 1 to 20 of 373

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967778inversion1nstd209human GRCh37.p13 chr17: 73,502,206-73,606,416 , GRCh38 chr17: 75,506,125-75,610,335 , LLGL2, 3 more genes
    nsv5929028copy number variation1nstd209human GRCh38 chr17: 75,546,589-75,546,804 , GRCh37.p13 chr17: 73,542,670-73,542,885 LLGL2
    nsv5704239mobile element insertion1nstd211human GRCh38 chr17: 75,560,832-75,560,832 , GRCh37.p13 chr17: 73,556,913-73,556,913 LLGL2
    nsv5645650insertion1nstd207human GRCh38 chr17: 75,558,923-75,558,923 , GRCh37.p13 chr17: 73,555,004-73,555,004 LLGL2
    nsv5594965copy number variation1nstd207human GRCh38 chr17: 75,558,806-75,558,885 , GRCh37.p13 chr17: 73,554,887-73,554,966 LLGL2
    nsv5585643copy number variation1nstd207human GRCh38 chr17: 75,546,566-75,546,781 , GRCh37.p13 chr17: 73,542,647-73,542,862 LLGL2
    nsv5530291copy number variation1nstd206human GRCh38 chr17: 75,528,233-75,533,117 , GRCh37.p13 chr17: 73,524,314-73,529,198 LLGL2
    nsv5392814copy number variation1nstd186human GRCh37 chr17: 73,542,664-73,542,930 , GRCh38.p12 chr17: 75,546,583-75,546,849 LLGL2
    nsv5391975copy number variation1nstd186human GRCh37 chr17: 73,542,637-73,543,016 , GRCh38.p12 chr17: 75,546,556-75,546,935 LLGL2
    nsv5349669translocation1nstd200human GRCh38 chr17: 75,565,649-75,565,649 , GRCh38 chr17: 75,565,581-75,565,581 , GRCh37.p13 chr17: 73,561,662-73,561,662 , GRCh37.p13 chr17: 73,561,730-73,561,730 LLGL2
    nsv5349668translocation1nstd200human GRCh38 chr17: 75,554,367-75,554,367 , GRCh38 chr17: 75,555,970-75,555,970 , GRCh37.p13 chr17: 73,550,448-73,550,448 , GRCh37.p13 chr17: 73,552,051-73,552,051 LLGL2
    nsv5293343copy number variation1nstd204human GRCh38.p13 chr17: 74,899,101-76,684,700 , GRCh37.p13 chr17: 72,895,199-74,680,782 , RNU6-24P, 92 more genes
    nsv5285796copy number variation1nstd204human GRCh37.p13 chr17: 73,542,682-73,669,280 , GRCh38.p13 chr17: 75,546,601-75,673,200 LLGL2, RECQL5, 5 more genes
    nsv5153028mobile element insertion1nstd203human GRCh38 chr17: 75,541,889-75,541,902 , GRCh37.p13 chr17: 73,537,970-73,537,983 LLGL2
    nsv5016702copy number variation1nstd200human GRCh38 chr17: 75,546,553-75,546,938 , GRCh37.p13 chr17: 73,542,634-73,543,019 LLGL2
    nsv4858986copy number variation1nstd200human GRCh37 chr17: 73,551,939-73,551,996 , GRCh38.p12 chr17: 75,555,858-75,555,915 LLGL2
    nsv4858985copy number variation1nstd200human GRCh37 chr17: 73,550,448-73,552,051 , GRCh38.p12 chr17: 75,554,367-75,555,970 LLGL2
    nsv4858984copy number variation1nstd200human GRCh37 chr17: 73,542,636-73,543,017 , GRCh38.p12 chr17: 75,546,555-75,546,936 LLGL2
    nsv4854394copy number variation1nstd200human GRCh37 chr17: 73,511,580-73,714,116 , GRCh38.p12 chr17: 75,515,499-75,718,036 , CASKIN2, 8 more genes
    nsv4745171copy number variation1nstd199human GRCh37 chr17: 73,542,617-73,542,839 , GRCh38.p12 chr17: 75,546,536-75,546,758 LLGL2
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