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Items: 1 to 20 of 159

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5897213copy number variation1nstd209human GRCh38 chr6: 41,595,312-41,596,626 , GRCh37.p13 chr6: 41,563,050-41,564,364 FOXP4
    nsv5845504copy number variation1nstd209human GRCh38 chr6: 41,595,431-41,596,665 , GRCh37.p13 chr6: 41,563,169-41,564,403 FOXP4
    nsv5674840mobile element insertion2nstd211human GRCh38 chr6: 41,560,933-41,560,933 , GRCh37.p13 chr6: 41,528,671-41,528,671 FOXP4
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5466214copy number variation1nstd206human GRCh38 chr6: 41,595,316-41,596,627 , GRCh37.p13 chr6: 41,563,054-41,564,365 FOXP4
    nsv5409681mobile element insertion1nstd206human GRCh38 chr6: 41,560,933-41,560,984 , GRCh37.p13 chr6: 41,528,671-41,528,722 FOXP4
    nsv5362892translocation1nstd200human GRCh38 chr6: 41,595,316-41,595,316 , GRCh38 chr6: 41,596,627-41,596,627 , GRCh37.p13 chr6: 41,563,054-41,563,054 , GRCh37.p13 chr6: 41,564,365-41,564,365 FOXP4
    nsv5336278translocation1nstd200human GRCh37 chr6: 41,564,365-41,564,365 , GRCh37 chr6: 41,563,054-41,563,054 , GRCh38.p12 chr6: 41,595,316-41,595,316 , GRCh38.p12 chr6: 41,596,627-41,596,627 FOXP4
    nsv5308405copy number variation1nstd204human GRCh38.p13 chr6: 41,595,293-41,596,650 , GRCh37.p13 chr6: 41,563,031-41,564,388 FOXP4
    nsv5238378copy number variation1nstd204human GRCh38.p13 chr6: 41,598,016-41,600,115 , GRCh37.p13 chr6: 41,565,754-41,567,853 MIR4641, FOXP4
    nsv5231600copy number variation1nstd204human GRCh38.p13 chr6: 41,595,181-41,596,715 , GRCh37.p13 chr6: 41,562,919-41,564,453 FOXP4
    nsv5228029copy number variation1nstd204human GRCh38.p13 chr6: 41,595,301-41,596,600 , GRCh37.p13 chr6: 41,563,039-41,564,338 FOXP4
    nsv5119334mobile element insertion1nstd203human GRCh38 chr6: 41,560,920-41,560,933 , GRCh37.p13 chr6: 41,528,658-41,528,671 FOXP4
    nsv4941072copy number variation1nstd200human GRCh38 chr6: 41,602,758-41,602,916 , GRCh37.p13 chr6: 41,570,496-41,570,654 FOXP4
    nsv4934662copy number variation1nstd200human GRCh38 chr6: 41,581,362-41,647,014 , GRCh37.p13 chr6: 41,549,100-41,614,752 MDFI, FOXP4, 1 more genes
    nsv4828663copy number variation1nstd200human GRCh37 chr6: 41,549,100-41,614,752 , GRCh38.p12 chr6: 41,581,362-41,647,014 MIR4641, FOXP4, 1 more genes
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4659977copy number variation1nstd186human GRCh37 chr6: 41,563,050-41,564,365 , GRCh38.p12 chr6: 41,595,312-41,596,627 FOXP4
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