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Items: 1 to 20 of 66

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4978112copy number variation1nstd200human GRCh38 chr11: 7,926,347-7,929,742 , GRCh37.p13 chr11: 7,947,894-7,951,289 OR10A6
    nsv4978110copy number variation1nstd200human GRCh38 chr11: 7,917,919-7,928,302 , GRCh37.p13 chr11: 7,939,466-7,949,849 OR10A6
    nsv4843521copy number variation1nstd200human GRCh37 chr11: 7,939,466-7,949,849 , GRCh38.p12 chr11: 7,917,919-7,928,302 , GRCh38.p12 chr11|NT_187583.1: 149,420-159,803 , GRCh38.p12 chr11|NW_011332695.1: 148,913-159,296 OR10A6
    nsv4832904copy number variation1nstd200human GRCh37 chr11: 7,947,894-7,951,289 , GRCh38.p12 chr11|NT_187583.1: 157,848-161,243 , GRCh38.p12 chr11: 7,926,347-7,929,742 , GRCh38.p12 chr11|NW_011332695.1: 157,341-160,736 OR10A6
    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
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4565647inversion1nstd166human GRCh37.p13 chr11: 6,776,274-9,026,287 , GRCh38.p12 chr11: 6,755,043-9,004,740 , ZNF215, 61 more genes
    nsv4370152copy number variation1nstd173human GRCh37 chr11: 6,629,042-8,085,652 , GRCh38.p12 chr11: 6,607,812-8,064,105 LOC105376533, GVINP2, 48 more genes
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 KRTAP5-3, OR56A7P, 457 more genes
    nsv4208841copy number variation1nstd166human GRCh37.p13 chr11: 7,939,466-7,949,849 , GRCh38.p12 chr11: 7,917,919-7,928,302 , GRCh38.p12 chr11|NW_011332695.1: 148,913-159,296 , GRCh38.p12 chr11|NT_187583.1: 149,420-159,803 OR10A6
    nsv4203642copy number variation1nstd166human GRCh37.p13 chr11: 7,947,894-7,951,289 , GRCh38.p12 chr11|NW_011332695.1: 157,341-160,736 , GRCh38.p12 chr11|NT_187583.1: 157,848-161,243 , GRCh38.p12 chr11: 7,926,347-7,929,742 OR10A6
    nsv3919565copy number variation1nstd102humanPathogenic GRCh38 chr11: 61,793-10,727,969 , GRCh37 chr11: 61,793-10,749,516 , NCBI36 chr11: 51,793-10,706,092 OR51A7, OR51F5P, 437 more genes
    nsv3913423copy number variation1nstd102humanUncertain significance NCBI36 chr11: 7,741,835-7,921,307 , GRCh37.p13 chr11: 7,785,259-7,964,731 , GRCh38.p12 chr11: 7,763,712-7,943,184 , GRCh38.p12 chr11|NT_187583.1: 1-174,685 , GRCh38.p12 chr11|NW_011332695.1: 1-174,178 OR10A3, OR5P1P, 8 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
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3906221copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673 PCNAP4, LIN7C, 688 more genes
    nsv3902973copy number variation1nstd102humanPathogenic GRCh37 chr11: 6,969,013-9,257,231 , GRCh38.p12 chr11: 6,947,782-9,235,684 NLRP14, NRIP3, 55 more genes
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