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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5917077copy number variation1nstd209human GRCh38 chr11: 56,773,521-56,777,685 , GRCh37.p13 chr11: 56,540,997-56,545,161 OR5G1P
    nsv5914325copy number variation1nstd209human GRCh38 chr11: 55,273,256-58,053,631 , GRCh37.p13 chr11: 55,040,732-57,821,103 , LOC107984365, 161 more genes
    nsv5908337copy number variation1nstd209human GRCh38 chr11: 56,725,760-56,944,763 , GRCh37.p13 chr11: 56,493,236-56,712,238 FADS2B, LOC105369310, 9 more genes
    nsv5863023copy number variation1nstd209human GRCh37.p13 chr11: 56,494,854-56,564,055 , GRCh38 chr11: 56,727,378-56,796,579 OR5G1P, OR9G3P, 4 more genes
    nsv5862644copy number variation2nstd209human GRCh38 chr11: 56,772,707-56,777,706 , GRCh37.p13 chr11: 56,540,183-56,545,182 OR5G1P
    nsv5498209copy number variation1nstd206human GRCh38 chr11: 56,773,522-56,777,686 , GRCh37.p13 chr11: 56,540,998-56,545,162 OR5G1P
    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
    nsv5355192translocation1nstd200human GRCh38 chr11: 56,777,686-56,777,686 , GRCh38 chr11: 56,773,522-56,773,522 , GRCh37.p13 chr11: 56,540,998-56,540,998 , GRCh37.p13 chr11: 56,545,162-56,545,162 OR5G1P
    nsv4838369copy number variation1nstd200human GRCh37 chr11: 56,540,998-56,545,162 , GRCh38.p12 chr11|NW_003871074.1: 91,364-95,528 , GRCh38.p12 chr11: 56,773,522-56,777,686 OR5G1P
    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
    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
    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
    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
    nsv4207233copy number variation1nstd166human GRCh37.p13 chr11: 56,529,610-56,590,163 , GRCh38.p12 chr11: 56,762,134-56,822,687 , GRCh38.p12 chr11|NW_003871074.1: 79,976-140,529 OR5G5P, LOC107987426, 3 more genes
    nsv4193072copy number variation1nstd166human GRCh37.p13 chr11: 56,540,998-56,545,162 , GRCh38.p12 chr11|NW_003871074.1: 91,364-95,528 , GRCh38.p12 chr11: 56,773,522-56,777,686 OR5G1P
    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
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