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Items: 1 to 20 of 196

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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
    nsv7009797copy number variation1nstd229human GRCh38 chr18: 35,966,849-35,977,500 , GRCh37.p13 chr18: 33,546,812-33,557,463 C18orf21, LOC105372066
    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
    nsv7001992copy number variation1nstd229human GRCh38 chr18: 35,973,960-35,977,705 , GRCh37.p13 chr18: 33,553,923-33,557,668 C18orf21
    nsv7001499copy number variation1nstd229human GRCh38 chr18: 35,968,219-35,970,852 , GRCh37.p13 chr18: 33,548,182-33,550,815 LOC105372066, C18orf21
    nsv7000294copy number variation1nstd229human GRCh38 chr18: 35,939,601-35,988,600 , GRCh37.p13 chr18: 33,519,564-33,568,563 C18orf21, LOC105372066, 1 more genes
    nsv6998963copy number variation1nstd229human GRCh38 chr18: 35,968,338-35,981,526 , GRCh37.p13 chr18: 33,548,301-33,561,489 RPRD1A, C18orf21, 1 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
    nsv6133335copy number variation1nstd213human GRCh37 chr18: 33,550,000-33,620,001 , GRCh38.p12 chr18: 35,970,037-36,040,038 RPRD1A, C18orf21, 1 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
    nsv5532370copy number variation1nstd206human GRCh38 chr18: 35,971,154-35,971,284 , GRCh37.p13 chr18: 33,551,117-33,551,247 LOC105372066, C18orf21
    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
    nsv5288206copy number variation1nstd204human GRCh38.p13 chr18: 35,979,128-35,980,481 , GRCh37.p13 chr18: 33,559,091-33,560,444 RPRD1A, C18orf21
    nsv5036576inversion1nstd200human GRCh38 chr18: 33,011,377-36,071,277 , GRCh37.p13 chr18: 30,591,341-33,651,240 , ZSCAN30, 25 more genes
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