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Items: 1 to 20 of 332

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050605inversion1nstd229human GRCh38 chr3: 154,113,488-154,143,973 , GRCh37.p13 chr3: 153,831,277-153,861,762 ARHGEF26-AS1, ARHGEF26
    nsv7047569inversion1nstd229human GRCh38 chr3: 152,490,812-161,531,961 , GRCh37.p13 chr3: 152,208,601-161,249,749 RPS2P19, LOC112268450, 128 more genes
    nsv7044966inversion1nstd229human GRCh38 chr3: 154,114,628-154,179,691 , GRCh37.p13 chr3: 153,832,417-153,897,480 ARHGEF26, ARHGEF26-AS1
    nsv6738074copy number variation1nstd229human GRCh38 chr3: 154,051,601-154,054,900 , GRCh37.p13 chr3: 153,769,390-153,772,689 ARHGEF26-AS1
    nsv6737363copy number variation1nstd229human GRCh38 chr3: 153,856,201-154,194,800 , GRCh37.p13 chr3: 153,573,990-153,912,589 RPL21P42, ARHGEF26-AS1, 1 more genes
    nsv6736725copy number variation1nstd229human GRCh38 chr3: 154,114,273-154,117,325 , GRCh37.p13 chr3: 153,832,062-153,835,114 ARHGEF26-AS1
    nsv6732134copy number variation1nstd229human GRCh38 chr3: 154,041,225-154,051,553 , GRCh37.p13 chr3: 153,759,014-153,769,342 ARHGEF26-AS1
    nsv6731647copy number variation1nstd229human GRCh38 chr3: 154,058,401-154,060,400 , GRCh37.p13 chr3: 153,776,190-153,778,189 ARHGEF26-AS1
    nsv6730583copy number variation1nstd229human GRCh38 chr3: 154,058,301-154,149,300 , GRCh37.p13 chr3: 153,776,090-153,867,089 ARHGEF26-AS1, ARHGEF26
    nsv6729506copy number variation1nstd229human GRCh38 chr3: 154,033,847-154,253,030 , GRCh37.p13 chr3: 153,751,636-153,970,819 LOC105374167, ARHGEF26-AS1, 1 more genes
    nsv6728246copy number variation1nstd229human GRCh38 chr3: 154,086,801-154,096,000 , GRCh37.p13 chr3: 153,804,590-153,813,789 ARHGEF26-AS1
    nsv6727606copy number variation1nstd229human GRCh38 chr3: 154,053,301-154,129,200 , GRCh37.p13 chr3: 153,771,090-153,846,989 ARHGEF26, ARHGEF26-AS1
    nsv6726028copy number variation1nstd229human GRCh38 chr3: 154,053,401-154,129,200 , GRCh37.p13 chr3: 153,771,190-153,846,989 ARHGEF26-AS1, ARHGEF26
    nsv6725542copy number variation1nstd229human GRCh38 chr3: 154,120,424-154,136,734 , GRCh37.p13 chr3: 153,838,213-153,854,523 ARHGEF26, ARHGEF26-AS1
    nsv6725464copy number variation1nstd229human GRCh38 chr3: 154,112,792-154,113,331 , GRCh37.p13 chr3: 153,830,581-153,831,120 ARHGEF26-AS1
    nsv6722947copy number variation1nstd229human GRCh38 chr3: 154,053,101-154,218,700 , GRCh37.p13 chr3: 153,770,890-153,936,489 ARHGEF26, ARHGEF26-AS1
    nsv6721965copy number variation1nstd229human GRCh38 chr3: 153,972,354-154,088,801 , GRCh37.p13 chr3: 153,690,143-153,806,590 RPL21P42, ARHGEF26-AS1
    nsv6720045copy number variation1nstd229human GRCh38 chr3: 153,534,883-154,120,064 , GRCh37.p13 chr3: 153,252,672-153,837,853 ARHGEF26-AS1, LINC02006, 2 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6568520inversion1nstd223human GRCh38 chr3: 154,053,725-154,054,637 , GRCh37.p13 chr3: 153,771,514-153,772,426 ARHGEF26-AS1
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