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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
    nsv6917151copy number variation1nstd229human GRCh38 chr11: 9,940,109-18,580,574 , GRCh37.p13 chr11: 9,961,656-18,602,121 MYOD1, MIR8070, 139 more genes
    nsv6912172copy number variation1nstd229human GRCh38 chr11: 11,164,849-11,787,312 , GRCh37.p13 chr11: 11,186,396-11,808,859 GALNT18, MIR4299, 7 more genes
    nsv6907855copy number variation1nstd229human GRCh38 chr11: 11,317,301-11,445,400 , GRCh37.p13 chr11: 11,338,848-11,466,947 CSNK2A3, GALNT18
    nsv6903513copy number variation1nstd229human GRCh38 chr11: 11,297,501-11,364,100 , GRCh37.p13 chr11: 11,319,048-11,385,647 CSNK2A3, GALNT18
    nsv6635893copy number variation1nstd227human GRCh37 chr11: 11,306,531-11,490,764 , GRCh38.p12 chr11: 11,284,984-11,469,217 CSNK2A3, GALNT18
    nsv6578417inversion1nstd223human GRCh38 chr11: 7,263,807-16,565,752 , GRCh37.p13 chr11: 7,285,038-16,587,299 TEAD1, IRAG1, 151 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
    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
    nsv4680073copy number variation1nstd189human GRCh37.p13 chr11: 11,168,594-11,762,796 , GRCh38.p12 chr11: 11,147,047-11,741,249 CSNK2A3, GALNT18, 7 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
    nsv4598762copy number variation1nstd183human GRCh37 chr11: 11,262,342-11,422,750 , GRCh38.p12 chr11: 11,240,795-11,401,203 GALNT18, CSNK2A3
    nsv4388405copy number variation1nstd173human GRCh37 chr11: 11,309,144-11,416,249 , GRCh38.p12 chr11: 11,287,597-11,394,702 CSNK2A3, GALNT18
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 KRTAP5-3, OR56A7P, 457 more genes
    nsv3971077copy number variation1nstd168human GRCh38 chr11: 11,306,808-11,371,839 , GRCh37.p13 chr11: 11,328,355-11,393,386 CSNK2A3, GALNT18
    nsv3969028insertion1nstd168human GRCh38 chr11: 11,204,697-11,371,839 , GRCh37.p13 chr11: 11,226,244-11,393,386 CSNK2A3, GALNT18, 2 more genes
    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
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