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Items: 1 to 20 of 214

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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
    nsv7095005copy number variation2nstd102humanUncertain significance GRCh37 chr18: 29,098,182-29,178,638 , GRCh38.p12 chr18: 31,518,219-31,598,675 DSG2, TTR, 1 more genes
    nsv7094931copy number variation1nstd102humanUncertain significance GRCh37 chr18: 29,078,215-29,178,638 , GRCh38.p12 chr18: 31,498,252-31,598,675 TTR, DSG2, 1 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
    nsv7008725copy number variation1nstd229human GRCh38 chr18: 31,564,477-31,620,320 , GRCh37.p13 chr18: 29,144,440-29,200,283 TTR, B4GALT6
    nsv7007149copy number variation1nstd229human GRCh38 chr18: 31,598,643-31,603,610 , GRCh37.p13 chr18: 29,178,606-29,183,573 TTR
    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
    nsv6624380copy number variation1nstd224human GRCh37 chr18: 29,111,449-29,226,444 , GRCh38.p12 chr18: 31,531,486-31,646,481 TTR, B4GALT6, 2 more genes
    nsv6528594copy number variation1nstd223human GRCh38 chr18: 31,586,886-31,596,427 , GRCh37.p13 chr18: 29,166,849-29,176,390 TTR
    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
    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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