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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070460inversion1nstd229human GRCh38 chr11: 21,520,035-27,618,155 , GRCh37.p13 chr11: 21,541,581-27,639,702 RPS25P1, LOC105376598, 48 more genes
    nsv7067025inversion1nstd229human GRCh38 chr11: 22,307,930-23,197,158 , GRCh37.p13 chr11: 22,329,476-23,218,704 SLC17A6, FANCF, 7 more genes
    nsv7058561inversion1nstd229human GRCh38 chr11: 22,022,654-22,865,606 , GRCh37.p13 chr11: 22,044,200-22,887,152 CCDC179, GAS2, 8 more genes
    nsv6917785copy number variation1nstd229human GRCh38 chr11: 22,813,734-23,250,365 , GRCh37.p13 chr11: 22,835,280-23,271,911 LINC02718, SVIP, 2 more genes
    nsv6917204copy number variation1nstd229human GRCh38 chr11: 22,785,727-22,891,902 , GRCh37.p13 chr11: 22,807,273-22,913,448 CCDC179, GAS2, 1 more genes
    nsv6915344copy number variation1nstd229human GRCh38 chr11: 22,814,730-22,859,866 , GRCh37.p13 chr11: 22,836,276-22,881,412 CCDC179, GAS2, 1 more genes
    nsv6914175copy number variation1nstd229human GRCh38 chr11: 22,846,660-22,846,779 , GRCh37.p13 chr11: 22,868,206-22,868,325 GAS2, CCDC179
    nsv6913490copy number variation1nstd229human GRCh38 chr11: 22,858,738-22,872,545 , GRCh37.p13 chr11: 22,880,284-22,894,091 GAS2, CCDC179
    nsv6913027copy number variation1nstd229human GRCh38 chr11: 22,853,933-22,854,031 , GRCh37.p13 chr11: 22,875,479-22,875,577 GAS2, CCDC179
    nsv6910953copy number variation1nstd229human GRCh38 chr11: 22,841,959-22,875,998 , GRCh37.p13 chr11: 22,863,505-22,897,544 GAS2, CCDC179
    nsv6909695copy number variation1nstd229human GRCh38 chr11: 22,711,857-22,896,122 , GRCh37.p13 chr11: 22,733,403-22,917,668 CCDC179, GAS2, 1 more genes
    nsv6906158copy number variation1nstd229human GRCh38 chr11: 18,831,701-26,837,040 , GRCh37.p13 chr11: 18,853,248-26,858,587 HTATIP2, LINC02686, 68 more genes
    nsv6905082copy number variation1nstd229human GRCh38 chr11: 22,837,205-23,297,654 , GRCh37.p13 chr11: 22,858,751-23,319,200 GAS2, CCDC179, 1 more genes
    nsv6901365copy number variation1nstd229human GRCh38 chr11: 22,773,846-22,904,003 , GRCh37.p13 chr11: 22,795,392-22,925,549 SVIP, CCDC179, 1 more genes
    nsv6637345copy number variation1nstd102humanUncertain significance GRCh37 chr11: 22,582,555-23,040,011 , GRCh38.p12 chr11: 22,561,009-23,018,465 SVIP, GAS2, 3 more genes
    nsv6634433copy number variation1nstd102humanUncertain significance GRCh37 chr11: 22,678,758-23,584,615 , GRCh38.p12 chr11: 22,657,212-23,563,069 CCDC179, RPS2P38, 8 more genes
    nsv6620913copy number variation1nstd224human GRCh37 chr11: 22,864,086-22,893,301 , GRCh38.p12 chr11: 22,842,540-22,871,755 GAS2, CCDC179
    nsv6455447copy number variation1nstd223human GRCh38 chr11: 22,813,734-23,250,365 , GRCh37.p13 chr11: 22,835,280-23,271,911 GAS2, CCDC179, 2 more genes
    nsv6438806copy number variation1nstd223human GRCh38 chr11: 22,841,959-22,875,997 , GRCh37.p13 chr11: 22,863,505-22,897,543 CCDC179, GAS2
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
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