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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
    nsv6112733copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,640,273-19,609,496 , GRCh38.p12 chr2: 15,500,149-19,409,735 LOC112267888, LOC105373454, 40 more genes
    nsv5686881mobile element insertion1nstd211human GRCh38 chr2: 17,917,367-17,917,367 , GRCh37.p13 chr2: 18,098,634-18,098,634 KCNS3
    nsv5623603insertion1nstd207human GRCh38 chr2: 17,919,608-17,919,608 , GRCh37.p13 chr2: 18,100,875-18,100,875 KCNS3
    nsv5620270insertion1nstd207human GRCh38 chr2: 17,887,011-17,887,011 , GRCh37.p13 chr2: 18,068,278-18,068,278 KCNS3
    nsv5440197copy number variation1nstd206human GRCh38 chr2: 17,750,919-18,037,345 , GRCh37.p13 chr2: 17,932,186-18,218,611 KCNS3, SMC6, 5 more genes
    nsv5399876mobile element insertion1nstd206human GRCh38 chr2: 17,917,367-17,917,418 , GRCh37.p13 chr2: 18,098,634-18,098,685 KCNS3
    nsv5288740copy number variation1nstd204human GRCh38.p13 chr2: 17,706,276-18,478,642 , GRCh37.p13 chr2: 17,887,543-18,659,908 KCNS3, SMC6, 7 more genes
    nsv5216150copy number variation1nstd204human GRCh38.p13 chr2: 17,930,845-17,931,944 , GRCh37.p13 chr2: 18,112,112-18,113,211 KCNS3
    nsv5215060copy number variation1nstd204human GRCh37.p13 chr2: 17,887,568-18,659,766 , GRCh38.p13 chr2: 17,706,301-18,478,500 KCNS3, SMC6, 7 more genes
    nsv5212183copy number variation1nstd204human GRCh38.p13 chr2: 17,890,803-17,892,160 , GRCh37.p13 chr2: 18,072,070-18,073,427 KCNS3
    nsv5206830copy number variation1nstd204human GRCh38.p13 chr2: 17,928,445-17,930,244 , GRCh37.p13 chr2: 18,109,712-18,111,511 KCNS3
    nsv5205403copy number variation1nstd204human GRCh38.p13 chr2: 17,929,445-17,930,544 , GRCh37.p13 chr2: 18,110,712-18,111,811 KCNS3
    nsv4904814copy number variation1nstd200human GRCh38 chr2: 17,750,919-18,037,345 , GRCh37.p13 chr2: 17,932,186-18,218,611 MSGN1, LOC105373449, 5 more genes
    nsv4900444copy number variation1nstd200human GRCh38 chr2: 17,912,490-17,913,466 , GRCh37.p13 chr2: 18,093,757-18,094,733 KCNS3
    nsv4788298copy number variation1nstd200human GRCh37 chr2: 17,932,186-18,218,611 , GRCh38.p12 chr2: 17,750,919-18,037,345 KCNS3, SMC6, 5 more genes
    nsv4775622copy number variation1nstd200human GRCh37 chr2: 18,093,757-18,094,733 , GRCh38.p12 chr2: 17,912,490-17,913,466 KCNS3
    nsv4728764copy number variation1nstd102humanUncertain significance GRCh37 chr2: 17,846,161-18,720,906 , GRCh38.p12 chr2: 17,664,894-18,539,640 MSGN1, SMC6, 7 more genes
    nsv4595121copy number variation1nstd183human GRCh37 chr2: 17,341,974-18,336,233 , GRCh38.p12 chr2: 17,160,707-18,154,967 KCNS3, LOC105373449, 12 more genes
    nsv4572139mobile element insertion1nstd166human GRCh37.p13 chr2: 18,106,688-18,106,688 , GRCh38.p12 chr2: 17,925,421-17,925,421 KCNS3
    nsv4465080mobile element insertion1nstd166human GRCh37.p13 chr2: 18,097,063-18,097,063 , GRCh38.p12 chr2: 17,915,796-17,915,796 KCNS3
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