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Items: 1 to 20 of 381

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148238copy number variation1nstd102humanPathogenic GRCh38 chr8: 115,586,904-135,607,135 , GRCh37.p13 chr8: 116,599,131-136,619,378 CCDC26, EFR3A, 238 more genes
    nsv7148132copy number variation1nstd102humanPathogenic GRCh37 chr8: 131,138,343-143,473,913 , GRCh38.p12 chr8: 130,126,097-142,392,552 LOC107983985, MIR30DHG, 104 more genes
    nsv7146133copy number variation1nstd232human GRCh37.p13 chr8: 133,758,676-133,758,733 , GRCh38.p12 chr8: 132,746,430-132,746,487 TMEM71
    nsv7144524copy number variation1nstd232human GRCh37.p13 chr8: 133,758,606-133,758,655 , GRCh38.p12 chr8: 132,746,360-132,746,409 TMEM71
    nsv7077533inversion1nstd229human GRCh38 chr8: 125,245,829-133,039,076 , GRCh37.p13 chr8: 126,258,071-134,051,321 PVT1, MTRF1LP2, 76 more genes
    nsv7073742inversion1nstd229human GRCh38 chr8: 132,711,868-132,711,902 , GRCh37.p13 chr8: 133,724,114-133,724,148 TMEM71
    nsv6853943copy number variation1nstd229human GRCh38 chr8: 132,711,801-132,722,200 , GRCh37.p13 chr8: 133,724,047-133,734,446 TMEM71
    nsv6852100copy number variation1nstd229human GRCh38 chr8: 132,595,470-132,801,758 , GRCh37.p13 chr8: 133,607,716-133,814,003 PHF20L1, LOC105375767, 2 more genes
    nsv6847147copy number variation1nstd229human GRCh38 chr8: 132,752,696-132,753,338 , GRCh37.p13 chr8: 133,764,942-133,765,584 TMEM71
    nsv6845472copy number variation1nstd229human GRCh38 chr8: 132,716,800-132,722,881 , GRCh37.p13 chr8: 133,729,046-133,735,127 TMEM71
    nsv6844737copy number variation1nstd229human GRCh38 chr8: 132,731,715-132,739,758 , GRCh37.p13 chr8: 133,743,961-133,752,004 TMEM71
    nsv6843306copy number variation1nstd229human GRCh38 chr8: 132,743,901-132,748,400 , GRCh37.p13 chr8: 133,756,147-133,760,646 TMEM71
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6569857inversion1nstd223human GRCh38 chr8: 132,756,881-132,757,549 , GRCh37.p13 chr8: 133,769,127-133,769,795 TMEM71
    nsv6568383inversion1nstd223human GRCh38 chr8: 132,756,916-132,757,541 , GRCh37.p13 chr8: 133,769,162-133,769,787 TMEM71
    nsv6565074inversion1nstd223human GRCh38 chr8: 132,757,079-132,757,556 , GRCh37.p13 chr8: 133,769,325-133,769,802 TMEM71
    nsv6428195copy number variation1nstd223human GRCh38 chr8: 132,745,301-132,746,000 , GRCh37.p13 chr8: 133,757,547-133,758,246 TMEM71
    nsv6424636copy number variation1nstd223human GRCh38 chr8: 132,752,690-132,753,337 , GRCh37.p13 chr8: 133,764,936-133,765,583 TMEM71
    nsv6416049copy number variation1nstd223human GRCh38 chr8: 132,712,901-132,719,300 , GRCh37.p13 chr8: 133,725,147-133,731,546 TMEM71
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
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