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Items: 1 to 20 of 230

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148101copy number variation1nstd102humanUncertain significance GRCh37 chr11: 118,373,113-118,430,576 , GRCh38.p12 chr11: 118,502,398-118,559,861 TTC36, RPL5P30, 4 more genes
    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
    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
    nsv6915118copy number variation1nstd229human GRCh38 chr11: 118,542,008-118,548,639 , GRCh37.p13 chr11: 118,412,723-118,419,354 , GRCh37.p13 chr11|NW_003871072.2: 167,446-174,077 IFT46, TMEM25
    nsv6914674copy number variation1nstd229human GRCh38 chr11: 118,563,189-118,563,221 , GRCh37.p13 chr11|NW_003871072.2: 188,627-188,659 , GRCh37.p13 chr11: 118,433,904-118,433,936 IFT46
    nsv6908726copy number variation1nstd229human GRCh38 chr11: 118,548,035-118,548,642 , GRCh37.p13 chr11: 118,418,750-118,419,357 , GRCh37.p13 chr11|NW_003871072.2: 173,473-174,080 IFT46
    nsv6908668copy number variation1nstd229human GRCh38 chr11: 118,574,639-118,574,837 , GRCh37.p13 chr11|NW_003871072.2: 200,077-200,275 , GRCh37.p13 chr11: 118,445,354-118,445,552 ARCN1, IFT46
    nsv6907260copy number variation1nstd229human GRCh38 chr11: 118,502,169-118,560,696 , GRCh37.p13 chr11|NW_003871072.2: 127,607-186,134 , GRCh37.p13 chr11: 118,372,884-118,431,411 TTC36-AS1, TTC36, 4 more genes
    nsv6902846copy number variation1nstd229human GRCh38 chr11: 118,558,584-118,559,846 , GRCh37.p13 chr11|NW_003871072.2: 184,022-185,284 , GRCh37.p13 chr11: 118,429,299-118,430,561 RPL5P30, IFT46
    nsv6901462copy number variation1nstd229human GRCh38 chr11: 118,540,870-118,544,003 , GRCh37.p13 chr11: 118,411,585-118,414,718 , GRCh37.p13 chr11|NW_003871072.2: 166,308-169,441 TMEM25, IFT46
    nsv6901156copy number variation1nstd229human GRCh38 chr11: 118,566,697-118,567,317 , GRCh37.p13 chr11|NW_003871072.2: 192,135-192,755 , GRCh37.p13 chr11: 118,437,412-118,438,032 IFT46
    nsv6899550copy number variation1nstd229human GRCh38 chr11: 118,573,995-118,632,034 , GRCh37.p13 chr11: 118,444,710-118,502,751 , GRCh37.p13 chr11|NW_003871072.2: 199,433-257,472 IFT46, PHLDB1, 2 more genes
    nsv6591863inversion1nstd223human GRCh38 chr11: 118,550,288-118,551,084 , GRCh37.p13 chr11|NW_003871072.2: 175,726-176,522 , GRCh37.p13 chr11: 118,421,003-118,421,799 IFT46
    nsv6588663inversion1nstd223human GRCh38 chr11: 118,568,333-118,568,930 , GRCh37.p13 chr11|NW_003871072.2: 193,771-194,368 , GRCh37.p13 chr11: 118,439,048-118,439,645 IFT46
    nsv6576998inversion1nstd223human GRCh38 chr11: 118,542,061-118,542,766 , GRCh37.p13 chr11|NW_003871072.2: 167,499-168,204 , GRCh37.p13 chr11: 118,412,776-118,413,481 TMEM25, IFT46
    nsv6473939copy number variation1nstd223human GRCh38 chr11: 118,540,862-118,543,999 , GRCh37.p13 chr11: 118,411,577-118,414,714 , GRCh37.p13 chr11|NW_003871072.2: 166,300-169,437 TMEM25, IFT46
    nsv6473605copy number variation1nstd223human GRCh38 chr11: 118,548,690-118,549,770 , GRCh37.p13 chr11|NW_003871072.2: 174,128-175,208 , GRCh37.p13 chr11: 118,419,405-118,420,485 IFT46
    nsv6467616copy number variation1nstd223human GRCh38 chr11: 118,548,159-118,548,606 , GRCh37.p13 chr11: 118,418,874-118,419,321 , GRCh37.p13 chr11|NW_003871072.2: 173,597-174,044 IFT46
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