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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7016794copy number variation1nstd229human GRCh38 chr18: 35,616,079-36,080,027 , GRCh37.p13 chr18: 33,196,043-33,659,990 NRBF2P1, RPRD1A, 7 more genes
    nsv7009293copy number variation1nstd229human GRCh38 chr18: 34,453,177-37,158,337 , GRCh37.p13 chr18: 32,033,141-34,738,300 LOC105372061, RNU4-3P, 31 more genes
    nsv6531154copy number variation1nstd223human GRCh38 chr18: 35,439,853-36,067,571 , GRCh37.p13 chr18: 33,019,817-33,647,534 LOC105372066, MIR187, 9 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
    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
    nsv6133334copy number variation1nstd213human GRCh37 chr18: 32,810,000-34,010,001 , GRCh38.p12 chr18: 35,230,036-36,430,038 GALNT1, ZNF24, 23 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
    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
    nsv6107779inversion1nstd212human GRCh38 chr18: 34,743,532-36,146,243 , GRCh37.p13 chr18: 32,323,496-33,726,206 , DTNA, 22 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
    nsv5036576inversion1nstd200human GRCh38 chr18: 33,011,377-36,071,277 , GRCh37.p13 chr18: 30,591,341-33,651,240 , ZSCAN30, 25 more genes
    nsv5011329copy number variation1nstd200human GRCh38 chr18: 35,439,844-36,067,579 , GRCh37.p13 chr18: 33,019,808-33,647,542 C18orf21, LOC105372065, 9 more genes
    nsv4871565inversion1nstd200human GRCh37 chr18: 30,591,341-33,651,241 , GRCh38.p12 chr18: 33,011,377-36,071,278 , LOC105372066, 25 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
    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
    nsv4336672sequence alteration1nstd166human GRCh37.p13 chr18: 21,176,191-70,772,863 , GRCh38.p12 chr18: 23,596,227-73,105,628 , CDH2, 557 more genes
    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
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