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Items: 1 to 20 of 281

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5955472insertion1nstd209human GRCh38 chr7: 77,334,579-77,334,579 , GRCh37.p13 chr7: 76,963,896-76,963,896 GSAP
    nsv5953265insertion1nstd209human GRCh38 chr7: 77,402,616-77,402,616 , GRCh37.p13 chr7: 77,031,933-77,031,933 GSAP
    nsv5911472copy number variation1nstd209human GRCh38 chr7: 77,392,183-77,392,508 , GRCh37.p13 chr7: 77,021,500-77,021,825 GSAP
    nsv5717602mobile element insertion1nstd211human GRCh38 chr7: 77,390,946-77,390,946 , GRCh37.p13 chr7: 77,020,263-77,020,263 GSAP
    nsv5692867mobile element insertion1nstd211human GRCh38 chr7: 77,330,593-77,330,593 , GRCh37.p13 chr7: 76,959,910-76,959,910 GSAP
    nsv5691449mobile element insertion1nstd211human GRCh38 chr7: 77,377,258-77,377,258 , GRCh37.p13 chr7: 77,006,575-77,006,575 , GSAP
    nsv5687149mobile element insertion2nstd211human GRCh38 chr7: 77,319,099-77,319,099 , GRCh37.p13 chr7: 76,948,416-76,948,416 GSAP
    nsv5685158mobile element insertion1nstd211human GRCh38 chr7: 77,366,909-77,366,909 , GRCh37.p13 chr7: 76,996,226-76,996,226 GSAP
    nsv5676096mobile element insertion1nstd211human GRCh38 chr7: 77,334,606-77,334,606 , GRCh37.p13 chr7: 76,963,923-76,963,923 GSAP
    nsv5675046mobile element insertion2nstd211human GRCh38 chr7: 77,351,460-77,351,460 , GRCh37.p13 chr7: 76,980,777-76,980,777 GSAP
    nsv5628069insertion1nstd207human GRCh38 chr7: 77,343,310-77,343,310 , GRCh37.p13 chr7: 76,972,627-76,972,627 GSAP
    nsv5628040insertion1nstd207human GRCh38 chr7: 77,351,448-77,351,448 , GRCh37.p13 chr7: 76,980,765-76,980,765 GSAP
    nsv5567661copy number variation1nstd207human GRCh38 chr7: 77,392,183-77,392,508 , GRCh37.p13 chr7: 77,021,500-77,021,825 GSAP
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5553835insertion1nstd206human GRCh38 chr7: 77,398,630-77,398,664 , GRCh37.p13 chr7: 77,027,947-77,027,981 GSAP
    nsv5487576copy number variation1nstd206human GRCh38 chr7: 77,340,082-77,345,596 , GRCh37.p13 chr7: 76,969,399-76,974,913 GSAP
    nsv5480995copy number variation1nstd206human GRCh38 chr7: 77,310,551-77,317,242 , GRCh37.p13 chr7: 76,939,868-76,946,559 GSAP
    nsv5480404copy number variation1nstd206human GRCh38 chr7: 77,392,163-77,392,529 , GRCh37.p13 chr7: 77,021,480-77,021,846 GSAP
    nsv5406869mobile element insertion1nstd206human GRCh38 chr7: 77,366,909-77,366,960 , GRCh37.p13 chr7: 76,996,226-76,996,277 GSAP
    nsv5400467mobile element insertion1nstd206human GRCh38 chr7: 77,319,099-77,319,150 , GRCh37.p13 chr7: 76,948,416-76,948,467 GSAP
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