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Items: 1 to 20 of 92

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7066313inversion1nstd229human GRCh38 chr11: 6,624,146-15,294,249 , GRCh37.p13 chr11: 6,645,377-15,315,795 RNA5SP332, TMEM41B, 163 more genes
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6915481copy number variation1nstd229human GRCh38 chr11: 7,014,782-7,919,611 , GRCh37.p13 chr11: 7,036,013-7,941,158 SYT9, OR10AB1P, 20 more genes
    nsv6914875copy number variation1nstd229human GRCh38 chr11: 7,662,701-7,813,700 , GRCh37.p13 chr11: 7,683,932-7,835,247 LOC105376533, PPFIBP2, 7 more genes
    nsv6906971copy number variation1nstd229human GRCh38 chr11: 6,634,801-9,831,623 , GRCh37.p13 chr11: 6,656,032-9,853,170 RIC3, LOC644656, 86 more genes
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6578417inversion1nstd223human GRCh38 chr11: 7,263,807-16,565,752 , GRCh37.p13 chr11: 7,285,038-16,587,299 TEAD1, IRAG1, 151 more genes
    nsv6442855copy number variation1nstd223human GRCh38 chr11: 6,634,801-9,831,623 , GRCh37.p13 chr11: 6,656,032-9,853,170 LOC105369149, C11orf16, 86 more genes
    nsv6437319copy number variation1nstd223human GRCh38 chr11: 7,714,633-7,908,708 , GRCh37.p13 chr11: 7,736,180-7,930,255 RPL7AP55, LOC107984307, 9 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6301112copy number variation1nstd186human GRCh37 chr11: 7,536,881-7,997,917 , GRCh38.p12 chr11: 7,515,650-7,976,370 RNU6-943P, OR5E1P, 17 more genes
    nsv6132276copy number variation1nstd213human GRCh37 chr11: 7,180,000-8,030,001 , GRCh38.p12 chr11: 7,158,769-8,008,454 PPFIBP2, EIF3F, 22 more genes
    nsv5718594mobile element insertion1nstd211human GRCh38 chr11: 7,727,208-7,727,208 , GRCh37.p13 chr11: 7,748,755-7,748,755 OR10AB1P
    nsv5500971copy number variation1nstd206human GRCh38 chr11: 7,515,650-7,976,370 , GRCh37.p13 chr11: 7,536,881-7,997,917 OR5P4P, RPL7AP55, 17 more genes
    nsv4978097copy number variation1nstd200human GRCh38 chr11: 7,722,109-7,728,830 , GRCh37.p13 chr11: 7,743,656-7,750,377 OR10AB1P
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    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
    nsv4676027copy number variation1nstd102humanUncertain significance GRCh37 chr11: 7,679,492-7,774,741 , GRCh38.p12 chr11: 7,658,261-7,753,194 OVCH2, OR10AB1P, 4 more genes
    nsv4675758copy number variation1nstd102humanLikely benign GRCh37 chr11: 7,670,248-7,797,257 , GRCh38.p12 chr11: 7,649,017-7,775,710 PPFIBP2, CYB5R2, 5 more genes
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