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Items: 1 to 20 of 190

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093833copy number variation6nstd102humanUncertain significance GRCh37 chr11: 116,691,583-121,500,272 , GRCh38.p12 chr11: 116,820,867-121,629,563 RN7SL688P, MIR4492, 131 more genes
    nsv7093753copy number variation1nstd102humanUncertain significance GRCh37 chr11: 117,209,303-120,133,495 , GRCh38.p12 chr11: 117,338,587-120,262,786 TMEM25, HYOU1, 93 more genes
    nsv7076724inversion1nstd229human GRCh38 chr11: 118,363,213-118,364,870 , GRCh37.p13 chr11: 118,233,928-118,235,585 UBE4A
    nsv7074550inversion1nstd229human GRCh38 chr11: 118,332,309-119,477,352 , GRCh37.p13 chr11: 118,203,024-119,348,063 VPS11, LOC100131626, 55 more genes
    nsv7062420inversion1nstd229human GRCh38 chr11: 117,681,463-119,526,734 , GRCh37.p13 chr11: 117,552,178-119,397,444 RN7SL688P, MIR4492, 72 more genes
    nsv6916845copy number variation1nstd229human GRCh38 chr11: 118,363,863-118,364,870 , GRCh37.p13 chr11: 118,234,578-118,235,585 UBE4A
    nsv6901346copy number variation1nstd229human GRCh38 chr11: 118,351,246-118,359,385 , GRCh37.p13 chr11: 118,221,961-118,230,100 UBE4A, CD3G
    nsv6577404inversion1nstd223human GRCh38 chr11: 118,393,778-118,395,035 , GRCh37.p13 chr11: 118,264,493-118,265,750 , GRCh37.p13 chr11|NW_003871072.2: 19,216-20,473 UBE4A, LOC100131626
    nsv6577191inversion1nstd223human GRCh38 chr11: 118,393,135-118,393,599 , GRCh37.p13 chr11: 118,263,850-118,264,314 , GRCh37.p13 chr11|NW_003871072.2: 18,573-19,037 LOC100131626, UBE4A
    nsv6576917inversion1nstd223human GRCh38 chr11: 118,377,461-118,377,641 , GRCh37.p13 chr11: 118,248,176-118,248,356 , GRCh37.p13 chr11|NW_003871072.2: 2,899-3,079 UBE4A
    nsv6461932copy number variation1nstd223human GRCh38 chr11: 118,363,859-118,364,869 , GRCh37.p13 chr11: 118,234,574-118,235,584 UBE4A
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6308962copy number variation1nstd102humanUncertain significance GRCh37 chr11: 116,660,844-121,500,272 , GRCh38.p12 chr11: 116,790,128-121,629,563 LOC107984399, PCSK7, 132 more genes
    nsv6304850copy number variation1nstd186human GRCh37 chr11: 118,234,575-118,235,503 , GRCh38.p12 chr11: 118,363,860-118,364,788 UBE4A
    nsv6291074copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847 ZW10, MPZL2, 378 more genes
    nsv6289927copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522 IGSF9B, MIR10526, 592 more genes
    nsv6258392mobile element insertion1nstd215human GRCh38 chr11: 118,387,256-118,387,256 , GRCh37.p13 chr11|NW_003871072.2: 12,694-12,694 , GRCh37.p13 chr11: 118,257,971-118,257,971 UBE4A, LOC100131626
    nsv6040369copy number variation1nstd212human GRCh38 chr11: 118,363,918-118,364,720 , GRCh37.p13 chr11: 118,234,633-118,235,435 UBE4A
    nsv6034258copy number variation1nstd212human GRCh38 chr11: 118,364,729-118,364,869 , GRCh37.p13 chr11: 118,235,444-118,235,584 UBE4A
    nsv5970277inversion1nstd209human GRCh38 chr11: 118,364,870-118,366,527 , GRCh37.p13 chr11: 118,235,585-118,237,242 UBE4A
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