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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5693008mobile element insertion1nstd211human GRCh38 chr6: 96,541,926-96,541,926 , GRCh37.p13 chr6: 96,989,802-96,989,802 UFL1
    nsv5683914mobile element insertion2nstd211human GRCh38 chr6: 96,531,643-96,531,643 , GRCh37.p13 chr6: 96,979,519-96,979,519 UFL1
    nsv5682746mobile element insertion1nstd211human GRCh38 chr6: 96,528,249-96,528,249 , GRCh37.p13 chr6: 96,976,125-96,976,125 UFL1
    nsv5473106copy number variation1nstd206human GRCh38 chr6: 96,554,431-96,554,624 , GRCh37.p13 chr6: 97,002,307-97,002,500 UFL1
    nsv5399338mobile element insertion1nstd206human GRCh38 chr6: 96,531,643-96,531,694 , GRCh37.p13 chr6: 96,979,519-96,979,570 UFL1
    nsv5394857mobile element insertion1nstd206human GRCh38 chr6: 96,528,249-96,528,300 , GRCh37.p13 chr6: 96,976,125-96,976,176 UFL1
    nsv5106084mobile element insertion1nstd203human GRCh38 chr6: 96,541,914-96,541,921 , GRCh37.p13 chr6: 96,989,790-96,989,797 UFL1
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4942370copy number variation1nstd200human GRCh38 chr6: 96,542,833-96,542,887 , GRCh37.p13 chr6: 96,990,709-96,990,763 UFL1
    nsv4685987copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 96,015,038-97,262,669 , GRCh38.p12 chr6: 95,567,162-96,814,793 FHL5, FUT9, 16 more genes
    nsv4617406copy number variation1nstd183human GRCh37 chr6: 97,001,607-97,006,693 , GRCh38.p12 chr6: 96,553,731-96,558,817 UFL1
    nsv4616951copy number variation1nstd183human GRCh37 chr6: 96,972,216-96,972,541 , GRCh38.p12 chr6: 96,524,340-96,524,665 UFL1
    nsv4611273copy number variation1nstd183human GRCh37 chr6: 96,981,984-96,984,075 , GRCh38.p12 chr6: 96,534,108-96,536,199 UFL1
    nsv4608427copy number variation1nstd183human GRCh37 chr6: 97,001,607-97,002,375 , GRCh38.p12 chr6: 96,553,731-96,554,499 UFL1
    nsv4606806copy number variation1nstd183human GRCh37 chr6: 96,981,984-96,982,292 , GRCh38.p12 chr6: 96,534,108-96,534,416 UFL1
    nsv4602356copy number variation1nstd183human GRCh37 chr6: 96,983,954-96,984,329 , GRCh38.p12 chr6: 96,536,078-96,536,453 UFL1
    nsv4486023mobile element insertion1nstd166human GRCh37.p13 chr6: 96,989,790-96,989,790 , GRCh38.p12 chr6: 96,541,914-96,541,914 UFL1
    nsv4480943mobile element insertion1nstd166human GRCh37.p13 chr6: 96,979,505-96,979,505 , GRCh38.p12 chr6: 96,531,629-96,531,629 UFL1
    nsv4455970copy number variation1nstd102humanUncertain significance GRCh37 chr6: 96,925,561-97,358,357 , GRCh38.p12 chr6: 96,477,685-96,910,481 LOC100286973, UFL1-AS1, 10 more genes
    nsv4385496copy number variation2nstd173human GRCh37 chr6: 93,036,907-97,776,208 , GRCh38.p12 chr6: 92,327,189-97,328,332 FUT9, LOC107986626, 34 more genes
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