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Items: 1 to 20 of 244

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095431copy number variation1nstd102humanUncertain significance GRCh37 chr18: 18,963,480-21,534,612 , GRCh38.p12 chr18: 21,383,519-23,954,648 MIB1, RN7SL233P, 41 more genes
    nsv7073318inversion1nstd229human GRCh38 chr18: 21,866,113-23,515,547 , GRCh37.p13 chr18: 19,446,074-21,095,511 RNA5SP451, GATA6, 26 more genes
    nsv7071697inversion1nstd229human GRCh38 chr18: 23,493,650-23,507,037 , GRCh37.p13 chr18: 21,073,614-21,087,001 RMC1, NPC1
    nsv7011102copy number variation1nstd229human GRCh38 chr18: 23,513,179-23,542,055 , GRCh37.p13 chr18: 21,093,143-21,122,019 RMC1, NPC1
    nsv7005597copy number variation1nstd229human GRCh38 chr18: 23,443,201-23,520,400 , GRCh37.p13 chr18: 21,023,165-21,100,364 RMC1, NPC1, 1 more genes
    nsv7005119copy number variation1nstd229human GRCh38 chr18: 23,494,609-23,741,871 , GRCh37.p13 chr18: 21,074,573-21,321,835 RPS10P27, RMC1, 4 more genes
    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
    nsv7000353copy number variation1nstd229human GRCh38 chr18: 23,491,696-23,504,067 , GRCh37.p13 chr18: 21,071,660-21,084,031 RMC1
    nsv6624578copy number variation1nstd224human GRCh37 chr18: 20,782,046-21,619,931 , GRCh38.p12 chr18: 23,202,082-24,039,967 LAMA3, RIOK3, 10 more genes
    nsv6624142copy number variation1nstd224human GRCh37 chr18: 21,067,076-21,089,164 , GRCh38.p12 chr18: 23,487,112-23,509,200 NPC1, RMC1
    nsv6585719inversion1nstd223human GRCh38 chr18: 23,517,960-23,518,308 , GRCh37.p13 chr18: 21,097,924-21,098,272 RMC1, NPC1
    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
    nsv6310250copy number variation1nstd102humanUncertain significance GRCh37 chr18: 21,112,166-21,153,558 , GRCh38.p12 chr18: 23,532,202-23,573,594 NPC1, RMC1
    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
    nsv6133436copy number variation1nstd213human GRCh37 chr18: 19,770,000-21,370,001 , GRCh38.p12 chr18: 22,190,039-23,790,037 GATA6, LAMA3, 21 more genes
    nsv5936701copy number variation1nstd209human GRCh38 chr18: 23,516,490-23,516,544 , GRCh37.p13 chr18: 21,096,454-21,096,508 RMC1, NPC1
    nsv5526270copy number variation1nstd206human GRCh38 chr18: 23,531,716-23,532,926 , GRCh37.p13 chr18: 21,111,680-21,112,890 RMC1, NPC1
    nsv5381258copy number variation1nstd102humanUncertain significance GRCh37 chr18: 21,112,146-21,166,327 , GRCh38.p12 chr18: 23,532,182-23,586,363 NPC1, RMC1
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