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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976130inversion1nstd209human GRCh38 chr11: 89,706,927-90,017,891 , GRCh37.p13 chr11: 89,440,095-89,751,059 TRIM49, UBTFL2, 18 more genes
    nsv5927479copy number variation1nstd209human GRCh38 chr11: 89,922,148-90,147,492 , GRCh37.p13 chr11: 89,655,316-89,880,660 LOC100128800, TRIM64EP, 10 more genes
    nsv5513420copy number variation1nstd206human GRCh38 chr11: 89,836,896-90,043,500 , GRCh37.p13 chr11: 89,570,064-89,776,668 ANKRD33BP9, TRIM51BP, 13 more genes
    nsv5506725copy number variation1nstd206human GRCh38 chr11: 89,854,896-90,017,896 , GRCh37.p13 chr11: 89,588,064-89,751,064 TRIM51EP, MTND1P35, 10 more genes
    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
    nsv5276509copy number variation1nstd204human GRCh38.p13 chr11: 89,964,701-89,970,700 , GRCh37.p13 chr11: 89,697,869-89,703,868 TRIM64
    nsv5274024copy number variation1nstd204human GRCh38.p13 chr11: 89,964,501-89,965,100 , GRCh37.p13 chr11: 89,697,669-89,698,268 TRIM64
    nsv5273451copy number variation1nstd204human GRCh38.p13 chr11: 89,962,301-89,965,000 , GRCh37.p13 chr11: 89,695,469-89,698,168 TRIM64
    nsv5272123copy number variation1nstd204human GRCh38.p13 chr11: 89,974,001-89,974,900 , GRCh37.p13 chr11: 89,707,169-89,708,068 TRIM64
    nsv5271897copy number variation1nstd204human GRCh38.p13 chr11: 89,971,801-89,973,500 , GRCh37.p13 chr11: 89,704,969-89,706,668 TRIM64
    nsv5267975copy number variation1nstd204human GRCh38.p13 chr11: 89,968,601-89,969,600 , GRCh37.p13 chr11: 89,701,769-89,702,768 TRIM64
    nsv5267124copy number variation1nstd204human GRCh38.p13 chr11: 89,955,901-89,967,300 , GRCh37.p13 chr11: 89,689,069-89,700,468 TRIM64
    nsv5265948copy number variation1nstd204human GRCh38.p13 chr11: 89,974,401-89,981,100 , GRCh37.p13 chr11: 89,707,569-89,714,268 ANKRD33BP9, TRIM51EP, 1 more genes
    nsv5264812copy number variation1nstd204human GRCh38.p13 chr11: 89,965,401-89,968,100 , GRCh37.p13 chr11: 89,698,569-89,701,268 TRIM64
    nsv5263640copy number variation1nstd204human GRCh38.p13 chr11: 89,967,601-89,968,100 , GRCh37.p13 chr11: 89,700,769-89,701,268 TRIM64
    nsv5263329copy number variation1nstd204human GRCh38.p13 chr11: 89,973,001-89,978,300 , GRCh37.p13 chr11: 89,706,169-89,711,468 TRIM64, ANKRD33BP9
    nsv5262583copy number variation1nstd204human GRCh38.p13 chr11: 89,949,601-89,998,200 , GRCh37.p13 chr11: 89,682,769-89,731,368 TRIM53AP, ANKRD33BP9, 2 more genes
    nsv5262496copy number variation1nstd204human GRCh38.p13 chr11: 89,966,701-89,967,000 , GRCh37.p13 chr11: 89,699,869-89,700,168 TRIM64
    nsv5261371copy number variation1nstd204human GRCh38.p13 chr11: 89,966,501-89,970,700 , GRCh37.p13 chr11: 89,699,669-89,703,868 TRIM64
    nsv4675846copy number variation1nstd102humanLikely benign GRCh37 chr11: 89,062,443-89,762,600 , GRCh38.p12 chr11: 89,329,275-90,029,432 TRIM64DP, LOC642579, 23 more genes
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