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Items: 1 to 20 of 298

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960279insertion1nstd209human GRCh38 chr2: 164,947,117-164,947,117 , GRCh37.p13 chr2: 165,803,627-165,803,627 SLC38A11
    nsv5681959mobile element insertion2nstd211human GRCh38 chr2: 164,933,025-164,933,025 , GRCh37.p13 chr2: 165,789,535-165,789,535 SLC38A11
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5445100copy number variation1nstd206human GRCh38 chr2: 164,731,077-165,066,763 , GRCh37.p13 chr2: 165,587,587-165,923,273 COBLL1, SLC38A11, 3 more genes
    nsv5434730copy number variation1nstd206human GRCh38 chr2: 148,693,148-164,933,481 , GRCh37.p13 chr2: 149,450,717-165,789,991 , RBM43, 205 more genes
    nsv5395599mobile element insertion1nstd206human GRCh38 chr2: 164,933,025-164,933,076 , GRCh37.p13 chr2: 165,789,535-165,789,586 SLC38A11
    nsv5350947translocation1nstd200human GRCh38 chr2: 164,915,332-164,915,332 , GRCh38 chr2: 164,915,219-164,915,219 , GRCh37.p13 chr2: 165,771,729-165,771,729 , GRCh37.p13 chr2: 165,771,842-165,771,842 SLC38A11
    nsv5327227inversion1nstd204human GRCh37.p13 chr2: 151,300,232-168,612,803 , GRCh38.p13 chr2: 150,443,718-167,756,293 , RND3, 198 more genes
    nsv5213642copy number variation1nstd204human GRCh38.p13 chr2: 164,945,728-164,947,827 , GRCh37.p13 chr2: 165,802,238-165,804,337 SLC38A11
    nsv5207597copy number variation1nstd204human GRCh38.p13 chr2: 164,945,028-164,947,377 , GRCh37.p13 chr2: 165,801,538-165,803,887 SLC38A11
    nsv5068736mobile element insertion1nstd203human GRCh38 chr2: 164,933,011-164,933,025 , GRCh37.p13 chr2: 165,789,521-165,789,535 SLC38A11
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4928851copy number variation1nstd200human GRCh38 chr2: 164,951,038-165,017,231 , GRCh37.p13 chr2: 165,807,548-165,873,741 SLC38A11
    nsv4928849copy number variation1nstd200human GRCh38 chr2: 164,769,781-165,091,565 , GRCh37.p13 chr2: 165,626,291-165,948,075 COBLL1, SLC38A11, 4 more genes
    nsv4926297copy number variation1nstd200human GRCh38 chr2: 164,932,439-164,937,269 , GRCh37.p13 chr2: 165,788,949-165,793,779 SLC38A11
    nsv4926296copy number variation1nstd200human GRCh38 chr2: 164,924,187-164,924,288 , GRCh37.p13 chr2: 165,780,697-165,780,798 SLC38A11
    nsv4926295copy number variation1nstd200human GRCh38 chr2: 164,923,455-164,924,843 , GRCh37.p13 chr2: 165,779,965-165,781,353 SLC38A11
    nsv4926294copy number variation1nstd200human GRCh38 chr2: 164,907,563-164,908,229 , GRCh37.p13 chr2: 165,764,073-165,764,739 SLC38A11
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