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Items: 1 to 20 of 302

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5947966insertion1nstd209human GRCh38 chr2: 171,363,796-171,363,796 , GRCh37.p13 chr2: 172,220,306-172,220,306 METTL8
    nsv5723915mobile element insertion1nstd211human GRCh38 chr2: 171,420,906-171,420,906 , GRCh37.p13 chr2: 172,277,416-172,277,416 METTL8
    nsv5689146mobile element insertion1nstd211human GRCh38 chr2: 171,375,554-171,375,554 , GRCh37.p13 chr2: 172,232,064-172,232,064 RPS26P20, METTL8
    nsv5687346mobile element insertion1nstd211human GRCh38 chr2: 171,385,382-171,385,382 , GRCh37.p13 chr2: 172,241,892-172,241,892 METTL8
    nsv5681981mobile element insertion2nstd211human GRCh38 chr2: 171,378,141-171,378,141 , GRCh37.p13 chr2: 172,234,651-172,234,651 METTL8
    nsv5680637mobile element insertion1nstd211human GRCh38 chr2: 171,430,532-171,430,532 , GRCh37.p13 chr2: 172,287,042-172,287,042 METTL8
    nsv5617515insertion1nstd207human GRCh38 chr2: 171,363,792-171,363,792 , GRCh37.p13 chr2: 172,220,302-172,220,302 METTL8
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5548781insertion1nstd206human GRCh38 chr2: 171,333,048-171,333,061 , GRCh37.p13 chr2: 172,189,558-172,189,571 METTL8
    nsv5536321insertion1nstd206human GRCh38 chr2: 171,360,533-171,360,538 , GRCh37.p13 chr2: 172,217,043-172,217,048 METTL8
    nsv5442271copy number variation1nstd206human GRCh38 chr2: 171,427,388-171,431,054 , GRCh37.p13 chr2: 172,283,898-172,287,564 METTL8
    nsv5411541mobile element insertion1nstd206human GRCh38 chr2: 171,385,382-171,385,433 , GRCh37.p13 chr2: 172,241,892-172,241,943 METTL8
    nsv5409183mobile element insertion1nstd206human GRCh38 chr2: 171,378,141-171,378,192 , GRCh37.p13 chr2: 172,234,651-172,234,702 METTL8
    nsv5403764mobile element insertion1nstd206human GRCh38 chr2: 171,375,554-171,375,605 , GRCh37.p13 chr2: 172,232,064-172,232,115 RPS26P20, METTL8
    nsv5381341copy number variation1nstd102humanPathogenic GRCh37 chr2: 171,999,572-182,774,361 , GRCh38.p12 chr2: 171,143,062-181,909,634 ALDH7A1P2, LOC101927055, 174 more genes
    nsv5381164copy number variation1nstd102humanUncertain significance GRCh37 chr2: 172,291,068-172,750,744 , GRCh38.p12 chr2: 171,434,558-171,894,234 SLC25A12, METTL8, 7 more genes
    nsv5341591translocation1nstd200human GRCh37 chr2: 172,221,745-172,221,745 , GRCh37 chr2: 172,220,555-172,220,555 , GRCh38.p12 chr2: 171,364,045-171,364,045 , GRCh38.p12 chr2: 171,365,235-171,365,235 METTL8
    nsv5339526translocation1nstd200human GRCh37 chr2: 172,222,247-172,222,247 , GRCh37 chr2: 172,220,556-172,220,556 , GRCh38.p12 chr2: 171,364,046-171,364,046 , GRCh38.p12 chr2: 171,365,737-171,365,737 METTL8
    nsv5077059mobile element insertion1nstd203human GRCh38 chr2: 171,320,395-171,320,404 , GRCh37.p13 chr2: 172,176,905-172,176,914 METTL8
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