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Items: 1 to 20 of 223

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970405insertion1nstd209human GRCh38 chr12: 9,093,829-9,093,829 , GRCh37.p13 chr12: 9,246,425-9,246,425 A2M, KLRG1
    nsv5721595mobile element insertion1nstd211human GRCh38 chr12: 9,084,673-9,084,673 , GRCh37.p13 chr12: 9,237,269-9,237,269 KLRG1, A2M
    nsv5708612mobile element insertion1nstd211human GRCh38 chr12: 9,114,660-9,114,660 , GRCh37.p13 chr12: 9,267,256-9,267,256 KLRG1, A2M
    nsv5704796mobile element insertion1nstd211human GRCh38 chr12: 9,083,632-9,083,632 , GRCh37.p13 chr12: 9,236,228-9,236,228 A2M, KLRG1
    nsv5649278insertion1nstd207human GRCh38 chr12: 9,093,829-9,093,829 , GRCh37.p13 chr12: 9,246,425-9,246,425 A2M, KLRG1
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5277554copy number variation1nstd204human GRCh38.p13 chr12: 9,067,271-9,069,270 , GRCh37.p13 chr12: 9,219,867-9,221,866 A2M, A2M-AS1, 1 more genes
    nsv5135132mobile element insertion1nstd203human GRCh38 chr12: 9,093,829-9,093,831 , GRCh37.p13 chr12: 9,246,425-9,246,427 A2M, KLRG1
    nsv5133463mobile element insertion1nstd203human GRCh38 chr12: 9,093,831-9,093,834 , GRCh37.p13 chr12: 9,246,427-9,246,430 A2M, KLRG1
    nsv5059963copy number variation1nstd102humanUncertain significance GRCh37 chr12: 9,245,491-9,245,492 , GRCh38 chr12: 9,092,895-9,092,896 A2M, KLRG1
    nsv5029743inversion1nstd200human GRCh38 chr12: 7,297,013-15,308,349 , GRCh37.p13 chr12: 7,449,609-15,461,283 , MIR1244-4, 259 more genes
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4727237insertion1nstd186human GRCh37 chr12: 9,246,426-9,246,426 , GRCh38.p12 chr12: 9,093,830-9,093,830 A2M, KLRG1
    nsv4722257insertion1nstd186human GRCh37 chr12: 9,246,425-9,246,425 , GRCh38.p12 chr12: 9,093,829-9,093,829 A2M, KLRG1
    nsv4684747insertion1nstd194human GRCh38.p12 chr12: 9,093,830-9,093,830 , GRCh37 chr12: 9,246,426-9,246,426 A2M, KLRG1
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
    nsv4616824copy number variation1nstd183human GRCh37 chr12: 8,488,721-9,625,223 , GRCh38.p12 chr12: 8,336,125-9,472,627 , BTG1P1, 43 more genes
    nsv4555958insertion1nstd166human GRCh37.p13 chr12: 9,246,425-9,246,425 , GRCh38.p12 chr12: 9,093,829-9,093,829 A2M, KLRG1
    nsv4506715mobile element insertion1nstd166human GRCh37.p13 chr12: 9,268,713-9,268,713 , GRCh38.p12 chr12: 9,116,117-9,116,117 A2M, KLRG1
    nsv4502215mobile element insertion1nstd166human GRCh37.p13 chr12: 9,256,548-9,256,548 , GRCh38.p12 chr12: 9,103,952-9,103,952 KLRG1, A2M
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