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Items: 1 to 20 of 369

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5972904insertion1nstd209human GRCh38 chr15: 50,340,891-50,340,891 , GRCh37.p13 chr15: 50,633,088-50,633,088 GABPB1
    nsv5852917copy number variation1nstd209human GRCh38 chr15: 50,324,624-50,331,527 , GRCh37.p13 chr15: 50,616,821-50,623,724 GABPB1
    nsv5713891mobile element insertion1nstd211human GRCh38 chr15: 50,292,729-50,292,729 , GRCh37.p13 chr15: 50,584,926-50,584,926 GABPB1
    nsv5711927mobile element insertion1nstd211human GRCh38 chr15: 50,346,606-50,346,606 , GRCh37.p13 chr15: 50,638,803-50,638,803 RNU6-94P, GABPB1
    nsv5698146mobile element insertion1nstd211human GRCh38 chr15: 50,314,186-50,314,186 , GRCh37.p13 chr15: 50,606,383-50,606,383 GABPB1
    nsv5698008mobile element insertion1nstd211human GRCh38 chr15: 50,292,525-50,292,525 , GRCh37.p13 chr15: 50,584,722-50,584,722 GABPB1
    nsv5654178insertion2nstd207human GRCh38 chr15: 50,340,887-50,340,887 , GRCh37.p13 chr15: 50,633,084-50,633,084 GABPB1
    nsv5599885copy number variation1nstd207human GRCh38 chr15: 50,340,852-50,340,923 , GRCh37.p13 chr15: 50,633,049-50,633,120 GABPB1
    nsv5531831copy number variation1nstd206human GRCh38 chr15: 50,343,317-50,343,789 , GRCh37.p13 chr15: 50,635,514-50,635,986 GABPB1
    nsv5524265copy number variation1nstd206human GRCh38 chr15: 50,281,457-50,285,683 , GRCh37.p13 chr15: 50,573,654-50,577,880 GABPB1
    nsv5421733mobile element insertion1nstd206human GRCh38 chr15: 50,292,729-50,292,780 , GRCh37.p13 chr15: 50,584,926-50,584,977 GABPB1
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5380079translocation1nstd200human GRCh38 chr15: 50,283,255-50,283,255 , GRCh38 chr15: 50,283,414-50,283,414 , GRCh37.p13 chr15: 50,575,611-50,575,611 , GRCh37.p13 chr15: 50,575,452-50,575,452 GABPB1
    nsv5380078translocation1nstd200human GRCh38 chr15: 50,283,413-50,283,413 , GRCh38 chr15: 50,283,107-50,283,107 , GRCh37.p13 chr15: 50,575,304-50,575,304 , GRCh37.p13 chr15: 50,575,610-50,575,610 GABPB1
    nsv5182560mobile element insertion1nstd203human GRCh38 chr15: 50,349,896-50,349,896 , GRCh37.p13 chr15: 50,642,093-50,642,093 GABPB1, GABPB1-IT1
    nsv5156338mobile element insertion1nstd203human GRCh38 chr15: 50,281,970-50,281,970 , GRCh37.p13 chr15: 50,574,167-50,574,167 GABPB1
    nsv5155365mobile element insertion1nstd203human GRCh38 chr15: 50,300,436-50,300,460 , GRCh37.p13 chr15: 50,592,633-50,592,657 GABPB1
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5007521copy number variation1nstd200human GRCh38 chr15: 50,343,818-50,347,013 , GRCh37.p13 chr15: 50,636,015-50,639,210 RNU6-94P, GABPB1-IT1, 1 more genes
    nsv5007520copy number variation1nstd200human GRCh38 chr15: 50,281,456-50,285,683 , GRCh37.p13 chr15: 50,573,653-50,577,880 GABPB1
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