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Items: 1 to 20 of 254

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5949324insertion1nstd209human GRCh38 chr2: 121,269,918-121,269,918 , GRCh37.p13 chr2: 122,027,494-122,027,494 TFCP2L1
    nsv5683103mobile element insertion1nstd211human GRCh38 chr2: 121,282,332-121,282,332 , GRCh37.p13 chr2: 122,039,908-122,039,908 TFCP2L1
    nsv5568591copy number variation1nstd207human GRCh38 chr2: 121,225,794-121,226,039 , GRCh37.p13 chr2: 121,983,370-121,983,615 TFCP2L1
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5557170sequence alteration1nstd206human GRCh38 chr2: 121,255,898-121,256,637 , GRCh37.p13 chr2: 122,013,474-122,014,213 TFCP2L1
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5449770copy number variation1nstd206human GRCh38 chr2: 121,237,364-121,237,440 , GRCh37.p13 chr2: 121,994,940-121,995,016 TFCP2L1
    nsv5440816copy number variation1nstd206human GRCh38 chr2: 121,225,796-121,226,085 , GRCh37.p13 chr2: 121,983,372-121,983,661 TFCP2L1
    nsv5382044copy number variation1nstd186human GRCh37 chr2: 121,983,416-121,983,660 , GRCh38.p12 chr2: 121,225,840-121,226,084 TFCP2L1
    nsv5361078translocation1nstd200human GRCh38 chr2: 121,237,440-121,237,440 , GRCh38 chr2: 121,237,364-121,237,364 , GRCh37.p13 chr2: 121,995,016-121,995,016 , GRCh37.p13 chr2: 121,994,940-121,994,940 TFCP2L1
    nsv5342865translocation1nstd200human GRCh37 chr2: 121,995,016-121,995,016 , GRCh37 chr2: 121,994,940-121,994,940 , GRCh38.p12 chr2: 121,237,364-121,237,364 , GRCh38.p12 chr2: 121,237,440-121,237,440 TFCP2L1
    nsv5074923mobile element insertion1nstd203human GRCh38 chr2: 121,220,861-121,220,874 , GRCh37.p13 chr2: 121,978,437-121,978,450 TFCP2L1
    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
    nsv4923906copy number variation1nstd200human GRCh38 chr2: 121,278,398-121,280,607 , GRCh37.p13 chr2: 122,035,974-122,038,183 TFCP2L1
    nsv4923904copy number variation1nstd200human GRCh38 chr2: 121,188,166-121,238,771 , GRCh37.p13 chr2: 121,945,742-121,996,347 TFCP2L1
    nsv4915303copy number variation1nstd200human GRCh38 chr2: 121,276,058-121,278,227 , GRCh37.p13 chr2: 122,033,634-122,035,803 TFCP2L1
    nsv4915302copy number variation1nstd200human GRCh38 chr2: 121,267,455-121,272,833 , GRCh37.p13 chr2: 122,025,031-122,030,409 TFCP2L1
    nsv4915301copy number variation1nstd200human GRCh38 chr2: 121,250,657-121,254,829 , GRCh37.p13 chr2: 122,008,233-122,012,405 TFCP2L1
    nsv4915300copy number variation1nstd200human GRCh38 chr2: 121,236,516-121,237,542 , GRCh37.p13 chr2: 121,994,092-121,995,118 TFCP2L1
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