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Items: 1 to 20 of 496

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6121335copy number variation1nstd186human GRCh37 chr9: 127,330,755-127,331,355 , GRCh38.p12 chr9: 124,568,476-124,569,076 NR6A1
    nsv5957857insertion1nstd209human GRCh38 chr9: 124,611,774-124,611,774 , GRCh37.p13 chr9: 127,374,053-127,374,053 NR6A1
    nsv5927447copy number variation1nstd209human GRCh38 chr9: 124,548,009-124,548,659 , GRCh37.p13 chr9: 127,310,288-127,310,938 NR6A1
    nsv5917533copy number variation1nstd209human GRCh38 chr9: 124,749,067-124,751,654 , GRCh37.p13 chr9: 127,511,346-127,513,933 NR6A1
    nsv5916215copy number variation1nstd209human GRCh38 chr9: 124,568,446-124,569,075 , GRCh37.p13 chr9: 127,330,725-127,331,354 NR6A1
    nsv5867439copy number variation1nstd209human GRCh38 chr9: 124,644,384-124,645,783 , GRCh37.p13 chr9: 127,406,663-127,408,062 NR6A1
    nsv5853907copy number variation1nstd209human GRCh38 chr9: 124,749,048-124,751,920 , GRCh37.p13 chr9: 127,511,327-127,514,199 NR6A1
    nsv5720961mobile element insertion2nstd211human GRCh38 chr9: 124,631,009-124,631,009 , GRCh37.p13 chr9: 127,393,288-127,393,288 NR6A1
    nsv5708298mobile element insertion1nstd211human GRCh38 chr9: 124,730,573-124,730,573 , GRCh37.p13 chr9: 127,492,852-127,492,852 NR6A1
    nsv5706860mobile element insertion1nstd211human GRCh38 chr9: 124,764,517-124,764,517 , GRCh37.p13 chr9: 127,526,796-127,526,796 NR6A1
    nsv5703888mobile element insertion1nstd211human GRCh38 chr9: 124,553,574-124,553,574 , GRCh37.p13 chr9: 127,315,853-127,315,853 NR6A1
    nsv5702512mobile element insertion2nstd211human GRCh38 chr9: 124,546,649-124,546,649 , GRCh37.p13 chr9: 127,308,928-127,308,928 NR6A1
    nsv5633042insertion1nstd207human GRCh38 chr9: 124,670,520-124,670,520 , GRCh37.p13 chr9: 127,432,799-127,432,799 NR6A1, MIR181A2HG
    nsv5594398copy number variation1nstd207human GRCh38 chr9: 124,579,144-124,579,277 , GRCh37.p13 chr9: 127,341,423-127,341,556 NR6A1
    nsv5593031copy number variation1nstd207human GRCh38 chr9: 124,568,446-124,569,075 , GRCh37.p13 chr9: 127,330,725-127,331,354 NR6A1
    nsv5563206sequence alteration1nstd206human GRCh38 chr9: 124,584,298-124,584,303 , GRCh37.p13 chr9: 127,346,577-127,346,582 NR6A1
    nsv5553002insertion1nstd206human GRCh38 chr9: 124,670,518-124,670,526 , GRCh37.p13 chr9: 127,432,797-127,432,805 NR6A1, MIR181A2HG
    nsv5552764insertion1nstd206human GRCh38 chr9: 124,653,431-124,653,467 , GRCh37.p13 chr9: 127,415,710-127,415,746 NR6A1
    nsv5536015insertion1nstd206human GRCh38 chr9: 124,584,298-124,584,298 , GRCh37.p13 chr9: 127,346,577-127,346,577 NR6A1
    nsv5490563copy number variation1nstd206human GRCh38 chr9: 124,683,198-124,683,339 , GRCh37.p13 chr9: 127,445,477-127,445,618 NR6A1, MIR181A2HG
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