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Items: 1 to 20 of 229

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975135inversion1nstd209human GRCh38 chr18: 10,627,041-12,196,370 , GRCh37.p13 chr18: 10,627,038-12,196,369 , GNAL, 28 more genes
    nsv5672896copy number variation1nstd102humanPathogenic GRCh37 chr18: 2,656,075-13,885,536 , GRCh38.p12 chr18: 2,656,076-13,885,537 RN7SL862P, LOC105371972, 181 more genes
    nsv5531356copy number variation1nstd206human GRCh38 chr18: 11,854,570-11,855,699 , GRCh37.p13 chr18: 11,854,569-11,855,698 GNAL, CHMP1B
    nsv5515716copy number variation1nstd206human GRCh38 chr18: 11,840,739-11,856,069 , GRCh37.p13 chr18: 11,840,738-11,856,068 GNAL, CHMP1B
    nsv5514907copy number variation1nstd206human GRCh38 chr18: 11,854,495-11,856,659 , GRCh37.p13 chr18: 11,854,494-11,856,658 CHMP1B, GNAL
    nsv5014283copy number variation1nstd200human GRCh38 chr18: 11,840,739-11,856,069 , GRCh37.p13 chr18: 11,840,738-11,856,068 CHMP1B, GNAL
    nsv4854546copy number variation1nstd200human GRCh37 chr18: 11,840,738-11,856,068 , GRCh38.p12 chr18: 11,840,739-11,856,069 CHMP1B, GNAL
    nsv4852097copy number variation1nstd200human GRCh37 chr18: 11,854,607-11,856,663 , GRCh38.p12 chr18: 11,854,608-11,856,664 GNAL, CHMP1B
    nsv4729915copy number variation1nstd102humanPathogenic GRCh37 chr18: 7,598,173-15,422,644 , GRCh38.p12 chr18: 7,598,175-15,410,899 CEP192, RNU2-27P, 155 more genes
    nsv4684313copy number variation1nstd102humanUncertain significance GRCh37 chr18: 10,140,629-12,236,187 , GRCh38.p12 chr18: 10,140,632-12,236,188 PIEZO2, LOC105371986, 38 more genes
    nsv4676393copy number variation1nstd102humanPathogenic GRCh37 chr18: 13,034-15,330,525 , GRCh38.p12 chr18: 13,034-15,330,526 PRELID3A, ANKRD30B, 275 more genes
    nsv4676314copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,304-15,143,714 , GRCh38.p12 chr18: 136,304-15,143,715 EIF4A2P1, PMM2P2, 263 more genes
    nsv4676159copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-13,894,429 , GRCh38.p12 chr18: 136,226-13,894,430 SLC25A51P2, BOLA2P1, 221 more genes
    nsv4676141copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-18,529,578 , GRCh38.p12 chr18: 136,226-20,949,617 ANKRD12, DLGAP1-AS1, 270 more genes
    nsv4626650copy number variation1nstd183human GRCh37 chr18: 10,593,600-11,923,379 , GRCh38.p12 chr18: 10,593,603-11,923,380 , MIX23P1, 22 more genes
    nsv4457793copy number variation1nstd102humanPathogenic GRCh37 chr18: 11,723,213-12,125,657 , GRCh38.p12 chr18: 11,723,214-12,125,658 SDHDP1, ASNSP6, 11 more genes
    nsv4385858copy number variation1nstd173human GRCh37 chr18: 136,227-18,529,578 , GRCh38.p12 chr18: 136,227-20,949,617 , LOC105371995, 276 more genes
    nsv4377411copy number variation1nstd173human GRCh37 chr18: 11,144,142-13,578,616 , GRCh38.p12 chr18: 11,144,143-13,578,617 , CHMP1B, 51 more genes
    nsv4369928copy number variation1nstd173human GRCh37 chr18: 11,146,695-13,578,616 , GRCh38.p12 chr18: 11,146,696-13,578,617 , RNU6-324P, 51 more genes
    nsv4365803copy number variation3nstd173human GRCh37 chr18: 11,146,560-13,578,616 , GRCh38.p12 chr18: 11,146,561-13,578,617 , SPIRE1, 51 more genes
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