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Items: 1 to 20 of 225

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5923252copy number variation1nstd209human GRCh38 chr10: 7,761,099-7,761,233 , GRCh37.p13 chr10: 7,803,062-7,803,196 KIN
    nsv5922254copy number variation1nstd209human GRCh38 chr10: 7,751,854-7,752,074 , GRCh37.p13 chr10: 7,793,817-7,794,037 KIN
    nsv5635679insertion1nstd207human GRCh38 chr10: 7,752,239-7,752,239 , GRCh37.p13 chr10: 7,794,202-7,794,202 KIN
    nsv5635266insertion1nstd207human GRCh38 chr10: 7,749,876-7,749,876 , GRCh37.p13 chr10: 7,791,839-7,791,839 ITIH2, KIN
    nsv5599500copy number variation1nstd207human GRCh38 chr10: 7,751,854-7,752,074 , GRCh37.p13 chr10: 7,793,817-7,794,037 KIN
    nsv5475434copy number variation1nstd206human GRCh38 chr10: 7,751,867-7,752,075 , GRCh37.p13 chr10: 7,793,830-7,794,038 KIN
    nsv5475376copy number variation1nstd206human GRCh38 chr10: 7,761,101-7,761,234 , GRCh37.p13 chr10: 7,803,064-7,803,197 KIN
    nsv5383794mobile element deletion2nstd186human GRCh37 chr10: 7,793,830-7,794,038 , GRCh38.p12 chr10: 7,751,867-7,752,075 KIN
    nsv5332747translocation1nstd200human GRCh37 chr10: 7,803,197-7,803,197 , GRCh37 chr10: 7,803,064-7,803,064 , GRCh38.p12 chr10: 7,761,101-7,761,101 , GRCh38.p12 chr10: 7,761,234-7,761,234 KIN
    nsv5205285mobile element deletion1nstd204human GRCh38.p13 chr10: 7,751,867-7,752,075 , GRCh37.p13 chr10: 7,793,830-7,794,038 KIN
    nsv5127489mobile element insertion1nstd203human GRCh38 chr10: 7,751,922-7,751,922 , GRCh37.p13 chr10: 7,793,885-7,793,885 KIN
    nsv5120246mobile element insertion1nstd203human GRCh38 chr10: 7,751,903-7,751,903 , GRCh37.p13 chr10: 7,793,866-7,793,866 KIN
    nsv4969500copy number variation1nstd200human GRCh38 chr10: 7,780,417-7,781,905 , GRCh37.p13 chr10: 7,822,380-7,823,868 KIN
    nsv4969499copy number variation1nstd200human GRCh38 chr10: 7,749,933-7,750,668 , GRCh37.p13 chr10: 7,791,896-7,792,631 KIN, ITIH2
    nsv4899486mobile element deletion1nstd200human GRCh38 chr10: 7,751,867-7,752,075 , GRCh37.p13 chr10: 7,793,830-7,794,038 KIN
    nsv4829911copy number variation1nstd200human GRCh37 chr10: 7,791,896-7,792,631 , GRCh38.p12 chr10: 7,749,933-7,750,668 ITIH2, KIN
    nsv4774754mobile element deletion1nstd200human GRCh37 chr10: 7,793,830-7,794,038 , GRCh38.p12 chr10: 7,751,867-7,752,075 KIN
    nsv4740635copy number variation1nstd199human GRCh37 chr10: 7,793,828-7,794,048 , GRCh38.p12 chr10: 7,751,865-7,752,085 KIN
    nsv4680619copy number variation1nstd189human GRCh38.p12 chr10: 7,641,648-7,769,175 , GRCh37.p13 chr10: 7,683,611-7,811,138 ITIH2, KIN, 1 more genes
    nsv4641621copy number variation1nstd186human GRCh37 chr10: 7,793,830-7,794,038 , GRCh38.p12 chr10: 7,751,867-7,752,075 KIN
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