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Items: 1 to 20 of 69

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112718copy number variation1nstd102humanUncertain significance GRCh38 chr11: 32,963,226-33,107,103 , GRCh37.p13 chr11: 32,984,772-33,128,649 DEPDC7, PIGCP1, 5 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv4986977copy number variation1nstd200human GRCh38 chr11: 33,073,838-33,076,145 , GRCh37.p13 chr11: 33,095,384-33,097,691 TCP11L1, LINC00294, 1 more genes
    nsv4984361copy number variation1nstd200human GRCh38 chr11: 33,074,841-33,429,641 , GRCh37.p13 chr11: 33,096,387-33,451,187 RPL29P23, CSTF3, 7 more genes
    nsv4984358copy number variation1nstd200human GRCh38 chr11: 32,982,087-33,532,736 , GRCh37.p13 chr11: 33,003,633-33,554,282 LOC105376615, TCP11L1, 9 more genes
    nsv4984357copy number variation1nstd200human GRCh38 chr11: 32,963,226-33,107,104 , GRCh37.p13 chr11: 32,984,772-33,128,650 CSTF3, PIGCP1, 5 more genes
    nsv4984356copy number variation1nstd200human GRCh38 chr11: 32,955,286-33,576,658 , GRCh37.p13 chr11: 32,976,832-33,598,204 TCP11L1, RPS24P15, 10 more genes
    nsv4832068copy number variation1nstd200human GRCh37 chr11: 32,976,832-33,598,204 , GRCh38.p12 chr11: 32,955,286-33,576,658 QSER1, DEPDC7, 10 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4728829copy number variation1nstd102humanUncertain significance GRCh37 chr11: 32,975,924-33,678,760 , GRCh38.p12 chr11: 32,954,378-33,657,214 RPS24P15, HIPK3, 11 more genes
    nsv4679549copy number variation1nstd189human GRCh37.p13 chr11: 33,040,951-33,512,841 , GRCh38.p12 chr11: 33,019,405-33,491,295 CSTF3, PIGCP1, 8 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4674824copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344 SNORA88, LINC02729, 305 more genes
    nsv4528028copy number variation1nstd166human GRCh37.p13 chr11: 33,028,243-33,103,473 , GRCh38.p12 chr11: 33,006,697-33,081,927 TCP11L1, LOC105376615, 3 more genes
    nsv4455873copy number variation1nstd102humanPathogenic GRCh37 chr11: 22,079,154-35,597,645 , GRCh38.p12 chr11: 22,057,608-35,576,097 DNAJC24, LOC102723568, 153 more genes
    nsv4413577copy number variation1nstd174human GRCh37 chr11: 32,969,258-33,586,535 , GRCh38.p12 chr11: 32,947,712-33,564,989 HIPK3, TCP11L1, 10 more genes
    nsv3922894copy number variation1nstd102humanUncertain significance NCBI36 chr11: 33,009,649-33,619,055 , GRCh37.p13 chr11: 33,053,073-33,662,479 , GRCh38.p12 chr11: 33,031,527-33,640,933 RPS24P15, TCP11L1, 8 more genes
    nsv3922794copy number variation1nstd102humanPathogenic GRCh37 chr11: 20,101,020-34,485,543 , GRCh38 chr11: 20,079,474-34,463,996 , NCBI36 chr11: 20,057,596-34,442,119 LOC107984419, LINC02758, 150 more genes
    nsv3922664copy number variation1nstd102humanPathogenic GRCh38 chr11: 22,550,115-38,199,159 , NCBI36 chr11: 22,528,237-38,177,285 , GRCh37 chr11: 22,571,661-38,220,709 CSTF3, LOC101928338, 170 more genes
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