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Items: 1 to 20 of 215

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966616insertion1nstd209human GRCh38 chr6: 63,674,283-63,674,283 , GRCh37.p13 chr6: 64,384,184-64,384,184 PHF3
    nsv5897476copy number variation1nstd209human GRCh38 chr6: 63,643,314-63,643,371 , GRCh37.p13 chr6: 64,353,219-64,353,276 PHF3
    nsv5889339copy number variation1nstd209human GRCh38 chr6: 63,676,623-63,678,368 , GRCh37.p13 chr6: 64,386,524-64,388,269 PHF3
    nsv5845692copy number variation1nstd209human GRCh38 chr6: 63,676,663-63,678,462 , GRCh37.p13 chr6: 64,386,564-64,388,363 PHF3
    nsv5692210mobile element insertion1nstd211human GRCh38 chr6: 63,715,968-63,715,968 , GRCh37.p13 chr6: 64,425,864-64,425,864 PHF3
    nsv5681263mobile element insertion2nstd211human GRCh38 chr6: 63,720,880-63,720,880 , GRCh37.p13 chr6: 64,430,776-64,430,776 EYS, PHF3
    nsv5675807mobile element insertion1nstd211human GRCh38 chr6: 63,644,152-63,644,152 , GRCh37.p13 chr6: 64,354,057-64,354,057 PHF3
    nsv5674243delins1nstd102humanPathogenic GRCh38 chr6: 63,720,724-63,721,012 , GRCh37 chr6: 64,430,620-64,430,908 PHF3, EYS
    nsv5673592copy number variation1nstd102humanPathogenic GRCh37 chr6: 64,431,075-64,431,154 , GRCh38 chr6: 63,721,179-63,721,258 PHF3, EYS
    nsv5643554insertion1nstd207human GRCh38 chr6: 63,674,283-63,674,283 , GRCh37.p13 chr6: 64,384,184-64,384,184 PHF3
    nsv5639347insertion1nstd207human GRCh38 chr6: 63,688,231-63,688,231 , GRCh37.p8 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN PHF3
    nsv5564440copy number variation1nstd102humanUncertain significance GRCh37 chr6: 64,413,426-64,454,916 , GRCh38.p12 chr6: 63,703,536-63,745,023 PHF3, EYS
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5534903insertion1nstd206human GRCh38 chr6: 63,674,290-63,674,290 , GRCh37.p13 chr6: 64,384,191-64,384,191 PHF3
    nsv5410979mobile element insertion1nstd206human GRCh38 chr6: 63,644,152-63,644,203 , GRCh37.p13 chr6: 64,354,057-64,354,108 PHF3
    nsv5401473mobile element insertion1nstd206human GRCh38 chr6: 63,720,880-63,720,931 , GRCh37.p13 chr6: 64,430,776-64,430,827 EYS, PHF3
    nsv5399802mobile element insertion1nstd206human GRCh38 chr6: 63,715,968-63,716,019 , GRCh37.p13 chr6: 64,425,864-64,425,915 PHF3
    nsv5363091translocation1nstd200human GRCh38 chr6: 63,715,471-63,715,471 , GRCh38 chr6: 63,715,403-63,715,403 , GRCh37.p13 chr6: 64,425,299-64,425,299 , GRCh37.p13 chr6: 64,425,367-64,425,367 PHF3
    nsv5110171mobile element insertion1nstd203human GRCh38 chr6: 63,715,956-63,715,968 , GRCh37.p13 chr6: 64,425,852-64,425,864 PHF3
    nsv5100511mobile element insertion1nstd203human GRCh38 chr6: 63,714,789-63,714,803 , GRCh37.p13 chr6: 64,424,685-64,424,699 PHF3
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