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Items: 1 to 20 of 413

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958035insertion1nstd209human GRCh38 chr5: 78,460,820-78,460,820 , GRCh37.p13 chr5: 77,756,643-77,756,643 SCAMP1
    nsv5952348insertion1nstd209human GRCh38 chr5: 78,430,203-78,430,203 , GRCh37.p13 chr5: 77,726,027-77,726,027 SCAMP1
    nsv5904437copy number variation1nstd209human GRCh38 chr5: 78,420,427-78,420,559 , GRCh37.p13 chr5: 77,716,251-77,716,383 SCAMP1
    nsv5902955copy number variation1nstd209human GRCh38 chr5: 78,465,183-78,468,159 , GRCh37.p13 chr5: 77,761,006-77,763,982 SCAMP1
    nsv5902936copy number variation1nstd209human GRCh38 chr5: 78,384,460-78,384,659 , GRCh37.p13 chr5: 77,680,284-77,680,483 SCAMP1
    nsv5902865copy number variation1nstd209human GRCh38 chr5: 78,392,021-78,392,070 , GRCh37.p13 chr5: 77,687,845-77,687,894 SCAMP1
    nsv5893282copy number variation1nstd209human GRCh38 chr5: 78,430,042-78,430,212 , GRCh37.p13 chr5: 77,725,866-77,726,036 SCAMP1
    nsv5842874copy number variation1nstd209human GRCh38 chr5: 78,465,103-78,468,122 , GRCh37.p13 chr5: 77,760,926-77,763,945 SCAMP1
    nsv5692679mobile element insertion2nstd211human GRCh38 chr5: 78,448,345-78,448,345 , GRCh37.p13 chr5: 77,744,169-77,744,169 SCAMP1
    nsv5687178mobile element insertion2nstd211human GRCh38 chr5: 78,374,673-78,374,673 , GRCh37.p13 chr5: 77,670,497-77,670,497 SCAMP1
    nsv5673667copy number variation1nstd102humanPathogenic GRCh37 chr5: 77,385,207-78,135,259 , GRCh38.p12 chr5: 78,089,383-78,839,436 ARSB, AP3B1, 6 more genes
    nsv5636307insertion1nstd207human GRCh38 chr5: 78,430,084-78,430,084 , GRCh37.p13 chr5: 77,725,908-77,725,908 SCAMP1
    nsv5634914insertion1nstd207human GRCh38 chr5: 78,460,820-78,460,820 , GRCh37.p13 chr5: 77,756,643-77,756,643 SCAMP1
    nsv5629287insertion1nstd207human GRCh38 chr5: 78,460,792-78,460,792 , GRCh37.p13 chr5: 77,756,615-77,756,615 SCAMP1
    nsv5628667insertion1nstd207human GRCh38 chr5: 78,448,100-78,448,100 , GRCh37.p13 chr5: 77,743,924-77,743,924 SCAMP1
    nsv5626156insertion1nstd207human GRCh38 chr5: 78,430,122-78,430,122 , GRCh37.p13 chr5: 77,725,946-77,725,946 SCAMP1
    nsv5625300insertion1nstd207human GRCh38 chr5: 78,430,103-78,430,103 , GRCh37.p13 chr5: 77,725,927-77,725,927 SCAMP1
    nsv5580379copy number variation1nstd207human GRCh38 chr5: 78,392,021-78,392,070 , GRCh37.p13 chr5: 77,687,845-77,687,894 SCAMP1
    nsv5570267copy number variation1nstd207human GRCh38 chr5: 78,430,042-78,430,212 , GRCh37.p13 chr5: 77,725,866-77,726,036 SCAMP1
    nsv5542896insertion1nstd206human GRCh38 chr5: 78,460,796-78,460,801 , GRCh37.p13 chr5: 77,756,619-77,756,624 SCAMP1
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