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Items: 1 to 20 of 311

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5881535copy number variation1nstd209human GRCh38 chr2: 102,109,357-102,109,421 , GRCh37.p13 chr2: 102,725,817-102,725,881 IL1R1
    nsv5684958mobile element insertion1nstd211human GRCh38 chr2: 102,138,950-102,138,950 , GRCh37.p13 chr2: 102,755,410-102,755,410 IL1R1
    nsv5578412copy number variation1nstd207human GRCh38 chr2: 102,109,357-102,109,421 , GRCh37.p13 chr2: 102,725,817-102,725,881 IL1R1
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5449986copy number variation1nstd206human GRCh38 chr2: 102,101,183-102,103,364 , GRCh37.p13 chr2: 102,717,643-102,719,824 IL1R1
    nsv5444140copy number variation1nstd206human GRCh38 chr2: 102,134,023-102,139,055 , GRCh37.p13 chr2: 102,750,483-102,755,515 IL1R1
    nsv5439863copy number variation1nstd206human GRCh38 chr2: 102,109,359-102,109,422 , GRCh37.p13 chr2: 102,725,819-102,725,882 IL1R1
    nsv5402785mobile element insertion1nstd206human GRCh38 chr2: 102,138,950-102,139,001 , GRCh37.p13 chr2: 102,755,410-102,755,461 IL1R1
    nsv5380551translocation1nstd200human GRCh38 chr2: 102,159,799-102,159,799 , GRCh38 chr2: 102,160,593-102,160,593 , GRCh37.p13 chr2: 102,776,259-102,776,259 , GRCh37.p13 chr2: 102,777,053-102,777,053 IL1R1
    nsv5360949translocation1nstd200human GRCh38 chr2: 102,156,931-102,156,931 , GRCh38 chr2: 102,157,545-102,157,545 , GRCh37.p13 chr2: 102,773,391-102,773,391 , GRCh37.p13 chr2: 102,774,005-102,774,005 IL1R1
    nsv5360948translocation1nstd200human GRCh38 chr2: 102,142,754-102,142,754 , GRCh38 chr2: 102,142,669-102,142,669 , GRCh37.p13 chr2: 102,759,129-102,759,129 , GRCh37.p13 chr2: 102,759,214-102,759,214 IL1R1
    nsv5343260translocation1nstd200human GRCh37 chr2: 102,777,047-102,777,047 , GRCh37 chr2: 102,776,390-102,776,390 , GRCh38.p12 chr2: 102,160,587-102,160,587 , GRCh38.p12 chr2: 102,159,930-102,159,930 IL1R1
    nsv5336320translocation1nstd200human GRCh37 chr2: 102,776,259-102,776,259 , GRCh37 chr2: 102,777,053-102,777,053 , GRCh38.p12 chr2: 102,160,593-102,160,593 , GRCh38.p12 chr2: 102,159,799-102,159,799 IL1R1
    nsv5334092translocation1nstd200human GRCh37 chr2: 102,686,424-102,686,424 , GRCh37 chr2: 102,686,358-102,686,358 , GRCh38.p12 chr2: 102,069,898-102,069,898 , GRCh38.p12 chr2: 102,069,964-102,069,964 IL1R1
    nsv5218777mobile element deletion1nstd204human GRCh38.p13 chr2: 102,132,961-102,133,265 , GRCh37.p13 chr2: 102,749,421-102,749,725 IL1R1
    nsv5190812mobile element insertion1nstd203human GRCh38 chr2: 102,073,904-102,073,917 , GRCh37.p13 chr2: 102,690,364-102,690,377 IL1R1
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4892986copy number variation1nstd200human GRCh38 chr2: 102,138,129-102,147,941 , GRCh37.p13 chr2: 102,754,589-102,764,401 IL1R1
    nsv4892985copy number variation1nstd200human GRCh38 chr2: 102,099,076-102,111,361 , GRCh37.p13 chr2: 102,715,536-102,727,821 IL1R1
    nsv4892984copy number variation1nstd200human GRCh38 chr2: 102,084,659-102,084,801 , GRCh37.p13 chr2: 102,701,119-102,701,261 IL1R1
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