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Items: 1 to 20 of 436

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5952043insertion1nstd209human GRCh38 chr2: 69,517,525-69,517,525 , GRCh37.p13 chr2: 69,744,657-69,744,657 RN7SL604P, AAK1
    nsv5948310insertion1nstd209human GRCh38 chr2: 69,493,158-69,493,158 , GRCh37.p13 chr2: 69,720,290-69,720,290 AAK1
    nsv5882821copy number variation1nstd209human GRCh38 chr2: 69,564,427-69,564,791 , GRCh37.p13 chr2: 69,791,559-69,791,923 AAK1
    nsv5874606copy number variation1nstd209human GRCh38 chr2: 69,500,976-69,501,046 , GRCh37.p13 chr2: 69,728,108-69,728,178 AAK1
    nsv5693563mobile element insertion1nstd211human GRCh38 chr2: 69,583,795-69,583,795 , GRCh37.p13 chr2: 69,810,927-69,810,927 AAK1
    nsv5681881mobile element insertion1nstd211human GRCh38 chr2: 69,508,345-69,508,345 , GRCh37.p13 chr2: 69,735,477-69,735,477 AAK1
    nsv5679156mobile element insertion2nstd211human GRCh38 chr2: 69,517,537-69,517,537 , GRCh37.p13 chr2: 69,744,669-69,744,669 AAK1, RN7SL604P
    nsv5609154insertion1nstd207human GRCh38 chr2: 69,517,525-69,517,525 , GRCh37.p13 chr2: 69,744,657-69,744,657 RN7SL604P, AAK1
    nsv5580934copy number variation1nstd207human GRCh38 chr2: 69,591,558-69,591,607 , GRCh37.p13 chr2: 69,818,690-69,818,739 AAK1
    nsv5554998sequence alteration1nstd206human GRCh38 chr2: 69,571,494-69,575,503 , GRCh37.p13 chr2: 69,798,626-69,802,635 AAK1
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5451968copy number variation1nstd206human GRCh38 chr2: 69,626,572-69,626,653 , GRCh37.p13 chr2: 69,853,704-69,853,785 AAK1
    nsv5450523copy number variation1nstd206human GRCh38 chr2: 69,479,166-69,480,788 , GRCh37.p13 chr2: 69,706,298-69,707,920 AAK1
    nsv5449363copy number variation1nstd206human GRCh38 chr2: 69,485,374-69,497,411 , GRCh37.p13 chr2: 69,712,506-69,724,543 AAK1
    nsv5447108copy number variation1nstd206human GRCh38 chr2: 69,562,811-69,564,064 , GRCh37.p13 chr2: 69,789,943-69,791,196 AAK1
    nsv5436109copy number variation1nstd206human GRCh38 chr2: 69,602,311-69,602,373 , GRCh37.p13 chr2: 69,829,443-69,829,505 AAK1
    nsv5434656copy number variation1nstd206human GRCh38 chr2: 69,569,259-69,569,334 , GRCh37.p13 chr2: 69,796,391-69,796,466 AAK1
    nsv5399323mobile element insertion1nstd206human GRCh38 chr2: 69,517,537-69,517,588 , GRCh37.p13 chr2: 69,744,669-69,744,720 AAK1, RN7SL604P
    nsv5394462mobile element insertion1nstd206human GRCh38 chr2: 69,508,345-69,508,396 , GRCh37.p13 chr2: 69,735,477-69,735,528 AAK1
    nsv5360761translocation1nstd200human GRCh38 chr2: 69,552,852-69,552,852 , GRCh38 chr2: 69,552,956-69,552,956 , GRCh37.p13 chr2: 69,779,984-69,779,984 , GRCh37.p13 chr2: 69,780,088-69,780,088 AAK1
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