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Items: 1 to 20 of 234

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5932483copy number variation1nstd209human GRCh38 chr14: 21,484,465-21,486,502 , GRCh37.p13 chr14: 21,952,624-21,954,661 TOX4
    nsv5929638copy number variation1nstd209human GRCh38 chr14: 21,494,333-21,494,474 , GRCh37.p13 chr14: 21,962,492-21,962,633 TOX4
    nsv5847765copy number variation1nstd209human GRCh38 chr14: 21,484,468-21,486,467 , GRCh37.p13 chr14: 21,952,627-21,954,626 TOX4
    nsv5712641mobile element insertion1nstd211human GRCh38 chr14: 21,488,080-21,488,080 , GRCh37.p13 chr14: 21,956,239-21,956,239 TOX4
    nsv5672730copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,756,136-22,005,055 , GRCh38.p12 chr14: 21,287,977-21,536,921 RAB2B, METTL3, 12 more genes
    nsv5593494copy number variation1nstd207human GRCh38 chr14: 21,484,465-21,486,501 , GRCh37.p13 chr14: 21,952,624-21,954,660 TOX4
    nsv5506506copy number variation1nstd206human GRCh38 chr14: 21,455,390-21,561,947 , GRCh37.p13 chr14: 21,923,549-22,030,078 SALL2, TOX4, 4 more genes
    nsv5497850copy number variation1nstd206human GRCh38 chr14: 21,484,465-21,486,503 , GRCh37.p13 chr14: 21,952,624-21,954,662 TOX4
    nsv5494783copy number variation1nstd206human GRCh38 chr14: 21,477,805-21,477,880 , GRCh37.p13 chr14: 21,945,964-21,946,039 TOX4
    nsv5357030translocation1nstd200human GRCh38 chr14: 21,487,033-21,487,033 , GRCh38 chr14: 21,486,951-21,486,951 , GRCh37.p13 chr14: 21,955,110-21,955,110 , GRCh37.p13 chr14: 21,955,192-21,955,192 TOX4
    nsv5306777copy number variation1nstd204human GRCh38.p13 chr14: 21,484,465-21,486,503 , GRCh37.p13 chr14: 21,952,624-21,954,662 TOX4
    nsv5274642copy number variation1nstd204human GRCh38.p13 chr14: 21,484,501-21,486,500 , GRCh37.p13 chr14: 21,952,660-21,954,659 TOX4
    nsv5274128copy number variation1nstd204human GRCh38.p13 chr14: 21,484,468-21,486,467 , GRCh37.p13 chr14: 21,952,627-21,954,626 TOX4
    nsv5273170copy number variation1nstd204human GRCh38.p13 chr14: 21,486,101-21,486,500 , GRCh37.p13 chr14: 21,954,260-21,954,659 TOX4
    nsv5271743copy number variation1nstd204human GRCh38.p13 chr14: 21,484,168-21,487,267 , GRCh37.p13 chr14: 21,952,327-21,955,426 TOX4
    nsv5267091copy number variation1nstd204human GRCh38.p13 chr14: 21,485,501-21,486,500 , GRCh37.p13 chr14: 21,953,660-21,954,659 TOX4
    nsv5266575copy number variation1nstd204human GRCh38.p13 chr14: 21,481,201-21,486,600 , GRCh37.p13 chr14: 21,949,360-21,954,759 TOX4
    nsv5262355copy number variation1nstd204human GRCh38.p13 chr14: 21,484,501-21,485,200 , GRCh37.p13 chr14: 21,952,660-21,953,359 TOX4
    nsv4990764copy number variation1nstd200human GRCh38 chr14: 21,484,465-21,486,503 , GRCh37.p13 chr14: 21,952,624-21,954,662 TOX4
    nsv4990763copy number variation1nstd200human GRCh38 chr14: 21,481,194-21,482,347 , GRCh37.p13 chr14: 21,949,353-21,950,506 TOX4
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