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Items: 1 to 20 of 335

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7069678inversion1nstd229human GRCh38 chr18: 26,899,186-27,010,741 , GRCh37.p13 chr18: 24,479,150-24,590,705 CHST9, ATP6V1E1P2, 1 more genes
    nsv7017632copy number variation1nstd229human GRCh38 chr18: 26,830,892-26,899,416 , GRCh37.p13 chr18: 24,410,856-24,479,380 AQP4-AS1, LOC440489, 1 more genes
    nsv7010036copy number variation1nstd229human GRCh38 chr18: 26,934,806-26,935,532 , GRCh37.p13 chr18: 24,514,770-24,515,496 AQP4-AS1, CHST9
    nsv7006929copy number variation1nstd229human GRCh38 chr18: 26,820,932-27,062,099 , GRCh37.p13 chr18: 24,400,896-24,642,063 AQP4, ATP6V1E1P2, 5 more genes
    nsv7005215copy number variation1nstd229human GRCh38 chr18: 26,918,730-26,920,581 , GRCh37.p13 chr18: 24,498,694-24,500,545 AQP4-AS1, CHST9
    nsv7001485copy number variation1nstd229human GRCh38 chr18: 23,020,759-30,428,209 , GRCh37.p13 chr18: 20,600,722-28,008,175 RN7SL97P, RIOK3, 76 more genes
    nsv6593973inversion1nstd223human GRCh38 chr18: 26,888,218-26,889,090 , GRCh37.p13 chr18: 24,468,182-24,469,054 AQP4-AS1
    nsv6532865copy number variation1nstd223human GRCh38 chr18: 26,899,853-26,907,183 , GRCh37.p13 chr18: 24,479,817-24,487,147 CHST9, AQP4-AS1
    nsv6532477copy number variation1nstd223human GRCh38 chr18: 26,885,017-26,885,430 , GRCh37.p13 chr18: 24,464,981-24,465,394 AQP4-AS1
    nsv6519394copy number variation1nstd223human GRCh38 chr18: 26,820,932-27,062,097 , GRCh37.p13 chr18: 24,400,896-24,642,061 AQP4, CHST9, 5 more genes
    nsv6517034copy number variation1nstd223human GRCh38 chr18: 26,876,564-26,877,162 , GRCh37.p13 chr18: 24,456,528-24,457,126 AQP4-AS1
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
    nsv6291786copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-25,252,276 , GRCh38.p12 chr18: 136,226-27,672,312 LOC107985122, LOC100130487, 375 more genes
    nsv6291540copy number variation1nstd102humanUncertain significance GRCh37 chr18: 18,611,942-26,843,691 , GRCh38.p12 chr18: 21,031,981-29,263,726 MIR133A1HG, LOC105372040, 111 more genes
    nsv6291503copy number variation1nstd102humanUncertain significance GRCh37 chr18: 23,050,629-26,026,370 , GRCh38.p12 chr18: 25,470,665-28,446,406 LOC440489, RN7SL97P, 32 more genes
    nsv6288984insertion1nstd214human GRCh38 chr18: 26,867,232-26,867,232 , GRCh37.p13 chr18: 24,447,196-24,447,196 AQP4-AS1
    nsv6259275mobile element insertion1nstd215human GRCh38 chr18: 26,896,878-26,896,878 , GRCh37.p13 chr18: 24,476,842-24,476,842 AQP4-AS1
    nsv6133380copy number variation1nstd213human GRCh37 chr18: 21,980,000-24,910,001 , GRCh38.p12 chr18: 24,400,036-27,330,037 NPM1P2, SS18, 39 more genes
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
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