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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5914325copy number variation1nstd209human GRCh38 chr11: 55,273,256-58,053,631 , GRCh37.p13 chr11: 55,040,732-57,821,103 , LOC107984365, 161 more genes
    nsv5555691sequence alteration1nstd206human GRCh38 chr11: 56,448,372-56,470,408 , GRCh37.p13 chr11: 56,215,848-56,237,884 OR5M4P, OR5M3, 1 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
    nsv4979459copy number variation1nstd200human GRCh38 chr11: 56,312,157-56,469,534 , GRCh37.p13 chr11: 56,079,633-56,237,010 OR8K1, OR5M4P, 12 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
    nsv4680588copy number variation1nstd189human GRCh37.p13 chr11: 55,444,212-57,222,540 , GRCh38.p12 chr11: 55,676,736-57,455,067 , APLNR, 109 more genes
    nsv4679448copy number variation1nstd189human GRCh37.p13 chr11: 54,793,898-56,426,206 , GRCh38.p12 chr11: 55,026,422-56,658,730 OR5D3P, OR5D2P, 98 more genes
    nsv4615331copy number variation1nstd183human GRCh37 chr11: 56,080,312-56,236,119 , GRCh38.p12 chr11: 56,312,836-56,468,643 OR8L1P, OR8K1, 12 more genes
    nsv4453292copy number variation1nstd102humannot provided GRCh37 chr11: 55,033,164-57,518,726 , GRCh38.p12 chr11: 55,265,688-57,751,254 OR8J3, LINC02735, 150 more genes
    nsv4415542copy number variation1nstd174human GRCh37 chr11: 56,078,073-56,237,487 , GRCh38.p12 chr11: 56,310,597-56,470,011 OR8K3, OR5AL1, 12 more genes
    nsv4384042copy number variation1nstd173human GRCh37 chr11: 55,212,270-56,906,448 , GRCh38.p12 chr11: 55,444,794-57,138,974 OR5BQ1P, OR5AL1, 111 more genes
    nsv4376896copy number variation1nstd173human GRCh37 chr11: 55,212,275-56,906,448 , GRCh38.p12 chr11: 55,444,799-57,138,974 OR5BP1P, FAM8A2P, 111 more genes
    nsv4367548copy number variation1nstd173human GRCh37 chr11: 56,079,967-56,236,887 , GRCh38.p12 chr11: 56,312,491-56,469,411 OR5M4P, OR8L1P, 12 more genes
    nsv4335068sequence alteration1nstd166human GRCh37.p13 chr11: 55,345,935-56,620,567 , GRCh38.p12 chr11: 55,578,459-56,853,091 OR5M6P, OR8L1P, 92 more genes
    nsv4212087copy number variation1nstd166human GRCh37.p13 chr11: 55,638,459-56,369,711 , GRCh38.p12 chr11: 55,870,983-56,602,235 OR5F2P, OR8K2P, 57 more genes
    nsv4208429copy number variation1nstd166human GRCh37.p13 chr11: 56,079,633-56,237,010 , GRCh38.p12 chr11: 56,312,157-56,469,534 OR8K1, OR5M4P, 12 more genes
    nsv3924646copy number variation1nstd102humanUncertain significance GRCh38 chr11: 55,316,535-57,539,457 , GRCh37 chr11: 55,084,011-57,306,930 , NCBI36 chr11: 54,840,587-57,063,506 OR5AL1, OR5AK2, 134 more genes
    nsv3924455copy number variation1nstd102humanBenign GRCh38 chr11: 55,445,689-57,114,783 , GRCh37 chr11: 55,213,165-56,882,257 , NCBI36 chr11: 54,969,741-56,638,833 OR5AL1, OR5F2P, 111 more genes
    nsv3919838copy number variation1nstd102humanBenign GRCh38 chr11: 56,149,822-56,770,518 , GRCh37 chr11: 55,917,298-56,537,994 , NCBI36 chr11: 55,673,874-56,294,570 OR2AH1P, LOC100129607, 46 more genes
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