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Items: 1 to 20 of 390

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906165copy number variation1nstd209human GRCh38 chr3: 190,572,850-190,573,146 , GRCh37.p13 chr3: 190,290,639-190,290,935 IL1RAP
    nsv5901954copy number variation1nstd209human GRCh38 chr3: 190,631,907-190,632,043 , GRCh37.p13 chr3: 190,349,696-190,349,832 IL1RAP
    nsv5896200copy number variation1nstd209human GRCh38 chr3: 190,621,819-190,621,921 , GRCh37.p13 chr3: 190,339,608-190,339,710 IL1RAP
    nsv5624343insertion1nstd207human GRCh38 chr3: 190,621,826-190,621,826 , GRCh37.p13 chr3: 190,339,615-190,339,615 IL1RAP
    nsv5584181copy number variation1nstd207human GRCh38 chr3: 190,572,850-190,573,146 , GRCh37.p13 chr3: 190,290,639-190,290,935 IL1RAP
    nsv5570808copy number variation1nstd207human GRCh38 chr3: 190,572,743-190,572,812 , GRCh37.p13 chr3: 190,290,532-190,290,601 IL1RAP
    nsv5555504sequence alteration1nstd206human GRCh38 chr3: 190,576,878-190,576,917 , GRCh37.p13 chr3: 190,294,667-190,294,706 IL1RAP
    nsv5539996insertion1nstd206human GRCh38 chr3: 190,578,256-190,578,289 , GRCh37.p13 chr3: 190,296,045-190,296,078 IL1RAP
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5444907copy number variation1nstd206human GRCh38 chr3: 190,572,861-190,573,147 , GRCh37.p13 chr3: 190,290,650-190,290,936 IL1RAP
    nsv5439635copy number variation1nstd206human GRCh38 chr3: 190,572,703-190,572,853 , GRCh37.p13 chr3: 190,290,492-190,290,642 IL1RAP
    nsv5438815copy number variation1nstd206human GRCh38 chr3: 190,621,819-190,621,925 , GRCh37.p13 chr3: 190,339,608-190,339,714 IL1RAP
    nsv5436031copy number variation1nstd206human GRCh38 chr3: 190,631,901-190,632,064 , GRCh37.p13 chr3: 190,349,690-190,349,853 IL1RAP
    nsv5383933mobile element deletion2nstd186human GRCh37 chr3: 190,290,650-190,290,936 , GRCh38.p12 chr3: 190,572,861-190,573,147 IL1RAP
    nsv5352342translocation1nstd200human GRCh38 chr3: 190,572,745-190,572,745 , GRCh38 chr3: 190,572,813-190,572,813 , GRCh37.p13 chr3: 190,290,534-190,290,534 , GRCh37.p13 chr3: 190,290,602-190,290,602 IL1RAP
    nsv5352341translocation1nstd200human GRCh38 chr3: 190,527,457-190,527,457 , GRCh38 chr3: 190,527,360-190,527,360 , GRCh37.p13 chr3: 190,245,246-190,245,246 , GRCh37.p13 chr3: 190,245,149-190,245,149 IL1RAP
    nsv5217319mobile element deletion1nstd204human GRCh38.p13 chr3: 190,572,861-190,573,147 , GRCh37.p13 chr3: 190,290,650-190,290,936 IL1RAP
    nsv5098412mobile element insertion1nstd203human GRCh38 chr3: 190,565,082-190,565,087 , GRCh37.p13 chr3: 190,282,871-190,282,876 IL1RAP
    nsv5092842mobile element insertion1nstd203human GRCh38 chr3: 190,572,881-190,572,883 , GRCh37.p13 chr3: 190,290,670-190,290,672 IL1RAP
    nsv5090078mobile element insertion1nstd203human GRCh38 chr3: 190,634,707-190,634,718 , GRCh37.p13 chr3: 190,352,496-190,352,507 IL1RAP
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