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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5509961copy number variation1nstd206human GRCh38 chr11: 13,682,645-13,691,191 , GRCh37.p13 chr11: 13,704,192-13,712,738 RPL39P26, FAR1
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv4984214copy number variation1nstd200human GRCh38 chr11: 13,638,158-13,688,294 , GRCh37.p13 chr11: 13,659,705-13,709,841 RPL39P26, FAR1
    nsv4978319copy number variation1nstd200human GRCh38 chr11: 13,730,470-13,731,729 , GRCh37.p13 chr11: 13,752,017-13,753,276 FAR1
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4674824copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344 SNORA88, LINC02729, 305 more genes
    nsv4607238copy number variation1nstd183human GRCh37 chr11: 13,735,365-13,736,018 , GRCh38.p12 chr11: 13,713,818-13,714,471 FAR1
    nsv4602405copy number variation1nstd183human GRCh37 chr11: 13,735,194-13,735,585 , GRCh38.p12 chr11: 13,713,647-13,714,038 FAR1
    nsv4599517copy number variation1nstd183human GRCh37 chr11: 13,739,420-13,776,421 , GRCh38.p12 chr11: 13,717,873-13,754,874 CENPUP1, FAR1
    nsv4496197mobile element insertion1nstd166human GRCh37.p13 chr11: 13,737,524-13,737,524 , GRCh38.p12 chr11: 13,715,977-13,715,977 FAR1
    nsv4487506mobile element insertion1nstd166human GRCh37.p13 chr11: 13,711,980-13,711,980 , GRCh38.p12 chr11: 13,690,433-13,690,433 FAR1
    nsv4486407mobile element insertion1nstd166human GRCh37.p13 chr11: 13,707,375-13,707,375 , GRCh38.p12 chr11: 13,685,828-13,685,828 FAR1, RPL39P26
    nsv4457247copy number variation1nstd102humanUncertain significance GRCh37 chr11: 13,635,916-13,752,798 , GRCh38.p12 chr11: 13,614,369-13,731,251 FAR1, RPL39P26
    nsv4456201copy number variation1nstd102humanUncertain significance GRCh37 chr11: 13,464,883-14,872,063 , GRCh38.p12 chr11: 13,443,336-14,850,517 COPB1, RNA5SP332, 18 more genes
    nsv4196164copy number variation1nstd166human GRCh37.p13 chr11: 13,686,000-13,695,000 , GRCh38.p12 chr11: 13,664,453-13,673,453 FAR1
    nsv3915585copy number variation1nstd102humanPathogenic NCBI36 chr11: 9,967,639-16,803,929 , GRCh37 chr11: 10,011,063-16,847,353 , GRCh38 chr11: 9,989,516-16,825,806 BTBD10, LOC107984370, 86 more genes
    nsv3912558copy number variation1nstd102humanPathogenic GRCh37 chr11: 446,754-18,926,289 , GRCh38 chr11: 446,754-18,904,742 , NCBI36 chr11: 436,754-18,882,865 TRIM22, CSNK2A3, 546 more genes
    nsv3912175copy number variation1nstd102humanPathogenic NCBI36 chr11: 10,107,142-14,047,625 , GRCh37.p13 chr11: 10,150,566-14,091,049 , GRCh38.p12 chr11: 10,129,019-14,069,502 LINC02545, CENPUP1, 58 more genes
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