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Items: 1 to 20 of 171

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6804227copy number variation1nstd229human GRCh38 chr6: 96,526,945-96,527,329 , GRCh37.p13 chr6: 96,974,821-96,975,205 UFL1
    nsv6636533copy number variation1nstd102humanPathogenic GRCh37 chr6: 96,596,732-105,554,568 , GRCh38.p12 chr6: 96,148,856-105,106,693 MCHR2-AS1, ACTG1P18, 65 more genes
    nsv6636338copy number variation1nstd102humanPathogenic GRCh37 chr6: 96,946,110-106,497,526 , GRCh38.p12 chr6: 96,498,234-106,049,651 BVES-AS1, LIN28B, 74 more genes
    nsv6634392copy number variation1nstd102humanUncertain significance GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297 MTHFD2P2, RPL7P27, 212 more genes
    nsv6631277copy number variation1nstd224human GRCh37 chr6: 95,390,186-97,681,784 , GRCh38.p12 chr6: 94,680,468-97,233,908 NDUFAF4, MANEA, 21 more genes
    nsv6616686copy number variation1nstd223human GRCh38 chr6: 96,541,201-96,542,200 , GRCh37.p13 chr6: 96,989,077-96,990,076 UFL1
    nsv6613102copy number variation1nstd223human GRCh38 chr6: 96,534,101-96,535,100 , GRCh37.p13 chr6: 96,981,977-96,982,976 UFL1
    nsv6610870copy number variation1nstd223human GRCh38 chr6: 96,550,399-96,550,943 , GRCh37.p13 chr6: 96,998,275-96,998,819 UFL1
    nsv6610120copy number variation1nstd223human GRCh38 chr6: 96,538,901-96,540,000 , GRCh37.p13 chr6: 96,986,777-96,987,876 UFL1
    nsv6602165copy number variation1nstd223human GRCh38 chr6: 96,519,903-96,521,081 , GRCh37.p13 chr6: 96,967,779-96,968,957 UFL1-AS1, UFL1
    nsv6415017copy number variation1nstd223human GRCh38 chr6: 96,442,864-96,721,420 , GRCh37.p13 chr6: 96,890,740-97,169,296 FHL5, UFL1, 6 more genes
    nsv6313858copy number variation1nstd102humanPathogenic GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488 RN7SL509P, LAMA4, 311 more genes
    nsv6290768copy number variation1nstd102humanUncertain significance GRCh37 chr6: 96,890,318-97,173,199 , GRCh38.p12 chr6: 96,442,442-96,725,323 FHL5, UFL1-AS1, 6 more genes
    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
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