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Items: 1 to 20 of 197

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5690564mobile element insertion1nstd211human GRCh38 chr6: 50,751,132-50,751,132 , GRCh37.p13 chr6: 50,718,845-50,718,845 TFAP2D
    nsv5680707mobile element insertion2nstd211human GRCh38 chr6: 50,744,441-50,744,441 , GRCh37.p13 chr6: 50,712,154-50,712,154 TFAP2D
    nsv5632546insertion1nstd207human GRCh38 chr6: 50,757,778-50,757,778 , GRCh37.p13 chr6: 50,725,491-50,725,491 TFAP2D
    nsv5628899insertion1nstd207human GRCh38 chr6: 50,747,843-50,747,843 , GRCh37.p13 chr6: 50,715,556-50,715,556 TFAP2D
    nsv5624573insertion1nstd207human GRCh38 chr6: 50,757,556-50,757,556 , GRCh37.p13 chr6: 50,725,269-50,725,269 TFAP2D
    nsv5574379copy number variation1nstd207human GRCh38 chr6: 50,757,729-50,757,805 , GRCh37.p13 chr6: 50,725,442-50,725,518 TFAP2D
    nsv5564761copy number variation1nstd207human GRCh38 chr6: 50,757,467-50,757,548 , GRCh37.p13 chr6: 50,725,180-50,725,261 TFAP2D
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5549431insertion1nstd206human GRCh38 chr6: 50,757,293-50,757,334 , GRCh37.p13 chr6: 50,725,006-50,725,047 TFAP2D
    nsv5472744copy number variation1nstd206human GRCh38 chr6: 50,757,370-50,757,673 , GRCh37.p13 chr6: 50,725,083-50,725,386 TFAP2D
    nsv5468927copy number variation1nstd206human GRCh38 chr6: 50,769,149-50,772,374 , GRCh37.p13 chr6: 50,736,862-50,740,087 TFAP2D
    nsv5467033copy number variation1nstd206human GRCh38 chr6: 50,730,775-50,731,998 , GRCh37.p13 chr6: 50,698,488-50,699,711 TFAP2D
    nsv5458877copy number variation1nstd206human GRCh38 chr6: 50,764,324-50,772,132 , GRCh37.p13 chr6: 50,732,037-50,739,845 TFAP2D
    nsv5397828mobile element insertion1nstd206human GRCh38 chr6: 50,751,132-50,751,183 , GRCh37.p13 chr6: 50,718,845-50,718,896 TFAP2D
    nsv5397818mobile element insertion1nstd206human GRCh38 chr6: 50,744,441-50,744,492 , GRCh37.p13 chr6: 50,712,154-50,712,205 TFAP2D
    nsv5116971mobile element insertion1nstd203human GRCh38 chr6: 50,766,679-50,766,682 , GRCh37.p13 chr6: 50,734,392-50,734,395 TFAP2D
    nsv5116735mobile element insertion1nstd203human GRCh38 chr6: 50,766,658-50,766,679 , GRCh37.p13 chr6: 50,734,371-50,734,392 TFAP2D
    nsv5116423mobile element insertion1nstd203human GRCh38 chr6: 50,766,655-50,766,679 , GRCh37.p13 chr6: 50,734,368-50,734,392 TFAP2D
    nsv5115893mobile element insertion1nstd203human GRCh38 chr6: 50,766,650-50,766,675 , GRCh37.p13 chr6: 50,734,363-50,734,388 TFAP2D
    nsv5109884mobile element insertion1nstd203human GRCh38 chr6: 50,766,641-50,766,679 , GRCh37.p13 chr6: 50,734,354-50,734,392 TFAP2D
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