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Items: 1 to 20 of 442

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962014insertion1nstd209human GRCh38 chr2: 217,809,560-217,809,560 , GRCh37.p13 chr2: 218,674,283-218,674,283 TNS1
    nsv5955348insertion1nstd209human GRCh38 chr2: 217,805,577-217,805,577 , GRCh37.p13 chr2: 218,670,300-218,670,300 TNS1
    nsv5954679insertion1nstd209human GRCh38 chr2: 217,937,078-217,937,078 , GRCh37.p13 chr2: 218,801,801-218,801,801 TNS1
    nsv5904224copy number variation1nstd209human GRCh38 chr2: 217,819,201-217,819,832 , GRCh37.p13 chr2: 218,683,924-218,684,555 TNS1
    nsv5897042copy number variation1nstd209human GRCh38 chr2: 217,922,894-217,923,046 , GRCh37.p13 chr2: 218,787,617-218,787,769 TNS1
    nsv5892464copy number variation1nstd209human GRCh38 chr2: 217,830,856-217,831,136 , GRCh37.p13 chr2: 218,695,579-218,695,859 TNS1
    nsv5687709mobile element insertion2nstd211human GRCh38 chr2: 217,937,091-217,937,091 , GRCh37.p13 chr2: 218,801,814-218,801,814 TNS1
    nsv5621908insertion1nstd207human GRCh38 chr2: 217,809,492-217,809,492 , GRCh37.p13 chr2: 218,674,215-218,674,215 TNS1
    nsv5618115insertion1nstd207human GRCh38 chr2: 217,809,396-217,809,396 , GRCh37.p13 chr2: 218,674,119-218,674,119 TNS1
    nsv5606362insertion1nstd207human GRCh38 chr2: 217,805,592-217,805,592 , GRCh37.p13 chr2: 218,670,315-218,670,315 TNS1
    nsv5570682copy number variation1nstd207human GRCh38 chr2: 217,809,260-217,809,312 , GRCh37.p13 chr2: 218,673,983-218,674,035 TNS1
    nsv5566793copy number variation1nstd207human GRCh38 chr2: 217,809,508-217,809,583 , GRCh37.p13 chr2: 218,674,231-218,674,306 TNS1
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5453561copy number variation1nstd206human GRCh38 chr2: 217,993,826-217,993,924 , GRCh37.p13 chr2: 218,858,549-218,858,647 TNS1
    nsv5446802copy number variation1nstd206human GRCh38 chr2: 217,894,645-217,894,757 , GRCh37.p13 chr2: 218,759,368-218,759,480 TNS1
    nsv5445170copy number variation1nstd206human GRCh38 chr2: 217,819,194-217,819,841 , GRCh37.p13 chr2: 218,683,917-218,684,564 TNS1
    nsv5440192copy number variation1nstd206human GRCh38 chr2: 217,830,856-217,831,137 , GRCh37.p13 chr2: 218,695,579-218,695,860 TNS1
    nsv5438726copy number variation1nstd206human GRCh38 chr2: 217,782,160-217,832,277 , GRCh37.p13 chr2: 218,646,883-218,697,000 TNS1, SNORA115
    nsv5400041mobile element insertion1nstd206human GRCh38 chr2: 217,937,091-217,937,135 , GRCh37.p13 chr2: 218,801,814-218,801,858 TNS1
    nsv5366828translocation1nstd200human GRCh38 chr2: 217,884,491-217,884,491 , GRCh38 chr2: 217,886,198-217,886,198 , GRCh37.p13 chr2: 218,749,214-218,749,214 , GRCh37.p13 chr2: 218,750,921-218,750,921 TNS1
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