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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
    nsv5974715insertion1nstd209human GRCh38 chr11: 33,148,534-33,148,534 , GRCh37.p13 chr11: 33,170,080-33,170,080 CSTF3
    nsv5697701mobile element insertion2nstd211human GRCh38 chr11: 33,095,822-33,095,822 , GRCh37.p13 chr11: 33,117,368-33,117,368 CSTF3
    nsv5656743insertion1nstd207human GRCh38 chr11: 33,148,534-33,148,534 , GRCh37.p13 chr11: 33,170,080-33,170,080 CSTF3
    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
    nsv5274172copy number variation1nstd204human GRCh38.p13 chr11: 33,116,701-33,125,600 , GRCh37.p13 chr11: 33,138,247-33,147,146 CSTF3
    nsv5139723mobile element insertion1nstd203human GRCh38 chr11: 33,148,537-33,148,547 , GRCh37.p13 chr11: 33,170,083-33,170,093 CSTF3
    nsv5139027mobile element insertion1nstd203human GRCh38 chr11: 33,148,536-33,148,547 , GRCh37.p13 chr11: 33,170,082-33,170,093 CSTF3
    nsv5137364mobile element insertion1nstd203human GRCh38 chr11: 33,127,065-33,127,067 , GRCh37.p13 chr11: 33,148,611-33,148,613 CSTF3
    nsv5135397mobile element insertion1nstd203human GRCh38 chr11: 33,148,539-33,148,547 , GRCh37.p13 chr11: 33,170,085-33,170,093 CSTF3
    nsv5133514mobile element insertion1nstd203human GRCh38 chr11: 33,148,540-33,148,547 , GRCh37.p13 chr11: 33,170,086-33,170,093 CSTF3
    nsv5131901mobile element insertion1nstd203human GRCh38 chr11: 33,128,745-33,128,762 , GRCh37.p13 chr11: 33,150,291-33,150,308 CSTF3
    nsv5128313mobile element insertion1nstd203human GRCh38 chr11: 33,148,538-33,148,547 , GRCh37.p13 chr11: 33,170,084-33,170,093 CSTF3
    nsv5125176mobile element insertion1nstd203human GRCh38 chr11: 33,127,060-33,127,067 , GRCh37.p13 chr11: 33,148,606-33,148,613 CSTF3
    nsv5124678mobile element insertion1nstd203human GRCh38 chr11: 33,106,244-33,106,259 , GRCh37.p13 chr11: 33,127,790-33,127,805 CSTF3
    nsv5123417mobile element insertion1nstd203human GRCh38 chr11: 33,148,547-33,148,553 , GRCh37.p13 chr11: 33,170,093-33,170,099 CSTF3
    nsv5123204mobile element insertion1nstd203human GRCh38 chr11: 33,148,534-33,148,547 , GRCh37.p13 chr11: 33,170,080-33,170,093 CSTF3
    nsv5121653mobile element insertion1nstd203human GRCh38 chr11: 33,148,541-33,148,547 , GRCh37.p13 chr11: 33,170,087-33,170,093 CSTF3
    nsv4984362copy number variation1nstd200human GRCh38 chr11: 33,104,504-33,193,237 , GRCh37.p13 chr11: 33,126,050-33,214,783 CSTF3, CSTF3-DT, 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
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