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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095440copy number variation1nstd102humanUncertain significance GRCh37 chr18: 28,647,981-29,648,347 , GRCh38.p12 chr18: 31,068,015-32,068,384 RNU6-167P, LOC390846, 22 more genes
    nsv7074645inversion1nstd229human GRCh38 chr18: 30,537,670-35,063,371 , GRCh37.p13 chr18: 28,117,636-32,643,335 DSC1, RN7SKP44, 46 more genes
    nsv7071421inversion1nstd229human GRCh38 chr18: 31,321,802-32,119,916 , GRCh37.p13 chr18: 28,901,765-29,699,879 TTR, B4GALT6, 20 more genes
    nsv7064867inversion1nstd229human GRCh38 chr18: 31,692,782-32,067,362 , GRCh37.p13 chr18: 29,272,745-29,647,325 LOC100421591, LOC390846, 10 more genes
    nsv7005193copy number variation1nstd229human GRCh38 chr18: 31,723,888-31,728,150 , GRCh37.p13 chr18: 29,303,851-29,308,113 LOC390846, B4GALT6, 1 more genes
    nsv6999674copy number variation1nstd229human GRCh38 chr18: 31,659,181-31,735,193 , GRCh37.p13 chr18: 29,239,144-29,315,156 LOC390846, LRRC37A7P, 2 more genes
    nsv6999196copy number variation1nstd229human GRCh38 chr18: 31,721,066-31,726,142 , GRCh37.p13 chr18: 29,301,029-29,306,105 LOC390846, LRRC37A7P, 1 more genes
    nsv6637941copy number variation1nstd102humanUncertain significance GRCh37 chr18: 29,152,719-29,422,344 , GRCh38.p12 chr18: 31,572,756-31,842,381 B4GALT6, LRRC37A7P, 5 more genes
    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
    nsv6314163copy number variation1nstd102humanUncertain significance GRCh37 chr18: 29,120,408-29,497,601 , GRCh38.p12 chr18: 31,540,445-31,917,638 LOC100421591, LOC390846, 8 more genes
    nsv6133439copy number variation1nstd213human GRCh37 chr18: 28,680,000-49,600,001 , GRCh38.p12 chr18: 31,100,037-52,073,631 ATP5F1A, DSC1, 240 more genes
    nsv6133333copy number variation1nstd213human GRCh37 chr18: 27,400,000-52,060,001 , GRCh38.p12 chr18: 29,820,035-54,532,766 ATP5F1A, DCC, 259 more genes
    nsv6133332copy number variation1nstd213human GRCh37 chr18: 24,970,000-32,810,001 , GRCh38.p12 chr18: 27,390,036-35,230,037 DSC2, DTNA, 61 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
    nsv5524785copy number variation1nstd206human GRCh38 chr18: 31,726,766-31,735,542 , GRCh37.p13 chr18: 29,306,729-29,315,505 LOC390846
    nsv5188613mobile element insertion1nstd203human GRCh38 chr18: 31,726,805-31,726,805 , GRCh37.p13 chr18: 29,306,768-29,306,768 LOC390846
    nsv5024038copy number variation1nstd200human GRCh38 chr18: 28,435,232-32,096,725 , GRCh37.p13 chr18: 26,015,196-29,676,688 DSC2, LOC100287539, 35 more genes
    nsv4729939copy number variation1nstd102humanUncertain significance GRCh37 chr18: 25,329,706-29,734,723 , GRCh38.p12 chr18: 27,749,742-32,154,760 SLC25A52, LOC105372043, 37 more genes
    nsv4729854copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,971,647-33,737,300 , GRCh38.p12 chr18: 26,391,683-36,157,337 CLUHP6, KLHL14, 100 more genes
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