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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129917insertion1nstd186human GRCh37 chr17: 74,724,388-74,724,439 , GRCh38.p12 chr17: 76,728,306-76,728,357 METTL23
    nsv5976712insertion1nstd209human GRCh38 chr17: 76,728,306-76,728,306 , GRCh37.p13 chr17: 74,724,388-74,724,388 METTL23
    nsv5936803copy number variation1nstd209human GRCh38 chr17: 76,732,086-76,732,230 , GRCh37.p13 chr17: 74,728,168-74,728,312 SRSF2, METTL23
    nsv5659613insertion1nstd207human GRCh38 chr17: 76,728,306-76,728,306 , GRCh37.p13 chr17: 74,724,388-74,724,388 METTL23
    nsv5648242insertion1nstd207human GRCh38 chr17: 76,731,539-76,731,539 , GRCh37.p13 chr17: 74,727,621-74,727,621 METTL23
    nsv5563569sequence alteration1nstd206human GRCh37.p13 chr17: 74,682,310-74,791,072 , GRCh38 chr17: 76,686,228-76,794,990 SRSF2, JMJD6, 6 more genes
    nsv5534101insertion1nstd206human GRCh38 chr17: 76,728,306-76,728,357 , GRCh37.p13 chr17: 74,724,388-74,724,439 METTL23
    nsv5283666copy number variation1nstd204human GRCh37.p13 chr17: 74,676,083-74,731,882 , GRCh38.p13 chr17: 76,680,001-76,735,800 SRSF2, JMJD6, 5 more genes
    nsv5016772copy number variation1nstd200human GRCh38 chr17: 76,734,039-76,743,570 , GRCh37.p13 chr17: 74,730,121-74,739,652 SRSF2, MFSD11, 2 more genes
    nsv4859042copy number variation1nstd200human GRCh37 chr17: 74,728,201-74,728,314 , GRCh38.p12 chr17: 76,732,119-76,732,232 SRSF2, METTL23
    nsv4725554insertion1nstd186human GRCh37 chr17: 74,724,388-74,724,388 , GRCh38.p12 chr17: 76,728,306-76,728,306 METTL23
    nsv4676341copy number variation1nstd102humanUncertain significance GRCh37 chr17: 74,509,193-75,602,123 , GRCh38.p12 chr17: 76,513,111-77,606,041 CYCSP40, RNU6-97P, 38 more genes
    nsv4676104copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963 LLGL2, TSEN54, 165 more genes
    nsv4654925copy number variation2nstd186human GRCh37 chr17: 74,728,202-74,728,313 , GRCh38.p12 chr17: 76,732,120-76,732,231 SRSF2, METTL23
    nsv4632383copy number variation1nstd183human GRCh37 chr17: 74,721,845-74,733,918 , GRCh38.p12 chr17: 76,725,763-76,737,836 MFSD11, METTL23, 3 more genes
    nsv4619567copy number variation1nstd183human GRCh37 chr17: 74,721,853-74,723,169 , GRCh38.p12 chr17: 76,725,771-76,727,087 METTL23, JMJD6
    nsv4563813sequence alteration1nstd166human GRCh37.p13 chr17: 74,682,236-74,791,072 , GRCh38.p12 chr17: 76,686,154-76,794,990 SRSF2, JMJD6, 6 more genes
    nsv4555154insertion1nstd166human GRCh37.p13 chr17: 74,724,388-74,724,388 , GRCh38.p12 chr17: 76,728,306-76,728,306 METTL23
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4268787copy number variation1nstd166human GRCh37.p13 chr17: 74,720,873-74,721,092 , GRCh38.p12 chr17: 76,724,791-76,725,010 JMJD6, METTL23
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