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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5293801copy number variation1nstd204human GRCh37.p13 chr18: 33,436,764-33,759,363 , GRCh38.p13 chr18: 35,856,801-36,179,400 SLC39A6, RPRD1A, 6 more genes
    nsv4676233copy number variation1nstd102humanPathogenic GRCh37 chr18: 22,868,759-34,335,753 , GRCh38.p12 chr18: 25,288,795-36,755,790 DHFRP1, CLUHP6, 116 more genes
    nsv4676192copy number variation1nstd102humanUncertain significance GRCh37 chr18: 33,384,923-34,561,159 , GRCh38.p12 chr18: 35,804,959-36,981,196 LOC105372071, ELP2, 15 more genes
    nsv4676155copy number variation1nstd102humanPathogenic GRCh37 chr18: 20,689,919-49,455,212 , GRCh38.p12 chr18: 23,109,955-51,928,842 KLHL14, RPL23AP77, 318 more genes
    nsv4350805copy number variation1nstd102humanPathogenic GRCh37 chr18: 33,554,981-36,939,357 , GRCh38.p12 chr18: 35,975,018-39,359,393 LOC101927879, LOC105372076, 28 more genes
    nsv4336672sequence alteration1nstd166human GRCh37.p13 chr18: 21,176,191-70,772,863 , GRCh38.p12 chr18: 23,596,227-73,105,628 , CDH2, 557 more genes
    nsv4262920copy number variation1nstd166human GRCh37.p13 chr18: 33,758,565-33,758,660 , GRCh38.p12 chr18: 36,178,602-36,178,697 ELP2, COSMOC
    nsv3924706copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097 LOC100420948, NPM1P2, 941 more genes
    nsv3924638copy number variation1nstd102humanPathogenic GRCh38 chr18: 20,962,119-74,691,446 , NCBI36 chr18: 16,796,078-70,532,390 , GRCh37 chr18: 18,542,080-72,403,402 HMGN1P30, LOC107985134, 596 more genes
    nsv3924351copy number variation1nstd102humanPathogenic NCBI36 chr18: 108,760-76,113,817 , GRCh38 chr18: 118,760-80,254,946 , GRCh37 chr18: 118,760-78,012,829 MIX23P1, LOC105372087, 942 more genes
    nsv3923838copy number variation1nstd102humanPathogenic NCBI36 chr18: 138,963-76,103,255 , GRCh37 chr18: 148,963-78,002,264 , GRCh38 chr18: 148,963-80,244,381 WDR7-OT1, HMGN1P30, 941 more genes
    nsv3920818copy number variation1nstd102humanPathogenic NCBI36 chr18: 15,370,696-76,117,153 , GRCh37.p13 chr18: 15,380,696-78,016,181 , GRCh38.p12 chr18: 15,380,697-80,258,298 AQP4-AS1, SERPINB8, 670 more genes
    nsv3920597copy number variation1nstd102humanUncertain significance GRCh37 chr18: 33,570,806-34,543,648 , GRCh38 chr18: 35,990,843-36,963,685 , NCBI36 chr18: 31,824,804-32,797,646 FHOD3, MOCOS, 10 more genes
    nsv3920302copy number variation1nstd102humanPathogenic NCBI36 chr18: 29,881,080-37,228,316 , GRCh38 chr18: 34,047,118-41,394,354 , GRCh37 chr18: 31,627,082-38,974,318 FHOD3, MIR3975, 61 more genes
    nsv3919896copy number variation1nstd102humanPathogenic GRCh38 chr18: 31,655,749-42,564,094 , NCBI36 chr18: 27,489,710-38,398,057 , GRCh37 chr18: 29,235,712-40,144,059 LOC107985168, NRBF2P1, 100 more genes
    nsv3919004copy number variation1nstd102humanPathogenic GRCh38 chr18: 136,226-80,256,240 , GRCh37 chr18: 136,226-78,014,123 , NCBI36 chr18: 126,226-76,115,097 LIVAR, LINC03069, 941 more genes
    nsv3918717copy number variation1nstd102humanPathogenic GRCh38 chr18: 35,097,761-39,379,288 , NCBI36 chr18: 30,931,723-35,213,250 , GRCh37 chr18: 32,677,725-36,959,252 LOC105372065, LOC105372068, 45 more genes
    nsv3918488copy number variation1nstd102humanPathogenic NCBI36 chr18: 43,345-76,068,860 , GRCh38 chr18: 53,345-80,209,986 , GRCh37 chr18: 53,345-77,967,869 LOC105372027, ASXL3, 945 more genes
    nsv3916426copy number variation1nstd102humanPathogenic GRCh37 chr18: 149,089-77,992,274 , NCBI36 chr18: 139,089-76,093,265 , GRCh38 chr18: 149,089-80,234,391 TPGS2, TWSG1-DT, 941 more genes
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