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Items: 1 to 20 of 236

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074145inversion1nstd229human GRCh38 chr11: 104,112,094-113,544,164 , GRCh37.p13 chr11: 103,982,822-113,414,886 COLCA1, LOC105369491, 150 more genes
    nsv7070377inversion1nstd229human GRCh38 chr11: 112,386,733-113,822,442 , GRCh37.p13 chr11: 112,257,456-113,693,164 RPS29P19, ZW10, 25 more genes
    nsv7069281inversion1nstd229human GRCh38 chr11: 107,936,485-114,400,629 , GRCh37.p13 chr11: 107,807,211-114,271,351 LRRC37A13P, POU2AF3, 121 more genes
    nsv7065935inversion1nstd229human GRCh38 chr11: 107,044,115-113,544,291 , GRCh37.p13 chr11: 106,914,841-113,415,013 LINC02762, TIMM8B, 112 more genes
    nsv7065476inversion1nstd229human GRCh38 chr11: 112,386,765-113,815,738 , GRCh37.p13 chr11: 112,257,488-113,686,460 TTC12, RPL23AP62, 24 more genes
    nsv6917485copy number variation1nstd229human GRCh38 chr11: 112,528,866-112,806,859 , GRCh37.p13 chr11: 112,399,589-112,677,582 LINC02764, LINC02763, 1 more genes
    nsv6915270copy number variation1nstd229human GRCh38 chr11: 112,528,201-112,539,600 , GRCh37.p13 chr11: 112,398,924-112,410,323 LINC02764, LINC02763
    nsv6914571copy number variation1nstd229human GRCh38 chr11: 112,529,146-112,543,888 , GRCh37.p13 chr11: 112,399,869-112,414,611 LINC02763, LINC02764
    nsv6914253copy number variation1nstd229human GRCh38 chr11: 112,470,101-112,509,600 , GRCh37.p13 chr11: 112,340,824-112,380,323 LINC02763, LOC107984389
    nsv6911179copy number variation1nstd229human GRCh38 chr11: 112,505,222-112,521,032 , GRCh37.p13 chr11: 112,375,945-112,391,755 LINC02763
    nsv6907282copy number variation1nstd229human GRCh38 chr11: 112,536,731-112,544,747 , GRCh37.p13 chr11: 112,407,454-112,415,470 LINC02763, LINC02764
    nsv6901519copy number variation1nstd229human GRCh38 chr11: 112,486,897-112,499,831 , GRCh37.p13 chr11: 112,357,620-112,370,554 LINC02763
    nsv6898987copy number variation1nstd229human GRCh38 chr11: 112,497,067-112,498,431 , GRCh37.p13 chr11: 112,367,790-112,369,154 LINC02763
    nsv6637811copy number variation1nstd102humanPathogenic GRCh37 chr11: 109,328,787-116,414,966 , GRCh38.p12 chr11: 109,458,061-116,544,249 LOC102723966, NXPE4, 129 more genes
    nsv6620697copy number variation1nstd224human GRCh37 chr11: 112,064,216-112,362,462 , GRCh38.p12 chr11: 112,193,493-112,491,739 MRPS36P4, PLET1, 12 more genes
    nsv6586218inversion1nstd223human GRCh38 chr11: 107,936,497-114,408,912 , GRCh37.p13 chr11: 107,807,223-114,279,634 LOC107984390, ATF4P4, 121 more genes
    nsv6579584inversion1nstd223human GRCh38 chr11: 112,519,072-112,519,659 , GRCh37.p13 chr11: 112,389,795-112,390,382 LINC02763
    nsv6577272inversion1nstd223human GRCh38 chr11: 112,531,443-112,533,057 , GRCh37.p13 chr11: 112,402,166-112,403,780 LINC02764, LINC02763
    nsv6472750copy number variation1nstd223human GRCh38 chr11: 112,497,067-112,498,426 , GRCh37.p13 chr11: 112,367,790-112,369,149 LINC02763
    nsv6468840copy number variation1nstd223human GRCh38 chr11: 112,514,266-112,514,742 , GRCh37.p13 chr11: 112,384,989-112,385,465 LINC02763
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