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Items: 1 to 20 of 297

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6122201copy number variation1nstd186human GRCh37 chr10: 6,097,386-6,097,868 , GRCh38.p12 chr10: 6,055,423-6,055,905 IL2RA
    nsv5959357insertion1nstd209human GRCh38 chr10: 6,042,148-6,042,148 , GRCh37.p13 chr10: 6,084,111-6,084,111 IL2RA
    nsv5927370copy number variation1nstd209human GRCh38 chr10: 6,055,799-6,055,849 , GRCh37.p13 chr10: 6,097,762-6,097,812 IL2RA
    nsv5920891copy number variation1nstd209human GRCh38 chr10: 6,055,407-6,055,904 , GRCh37.p13 chr10: 6,097,370-6,097,867 IL2RA
    nsv5919682copy number variation1nstd209human GRCh38 chr10: 6,022,805-6,022,877 , GRCh37.p13 chr10: 6,064,768-6,064,840 IL2RA
    nsv5672604copy number variation1nstd102humanPathogenic GRCh37 chr10: 120,001-6,920,000 , GRCh38.p12 chr10: 74,061-6,878,038 PITRM1-AS1, TRV-TAC3-1, 133 more genes
    nsv5643467insertion1nstd207human GRCh38 chr10: 6,055,839-6,055,839 , GRCh37.p13 chr10: 6,097,802-6,097,802 IL2RA
    nsv5625255insertion1nstd207human GRCh38 chr10: 6,031,446-6,031,446 , GRCh37.p13 chr10: 6,073,409-6,073,409 LOC107984201, IL2RA
    nsv5601114copy number variation1nstd207human GRCh38 chr10: 6,031,444-6,031,493 , GRCh37.p13 chr10: 6,073,407-6,073,456 LOC107984201, IL2RA
    nsv5597460copy number variation1nstd207human GRCh38 chr10: 6,022,805-6,022,877 , GRCh37.p13 chr10: 6,064,768-6,064,840 IL2RA
    nsv5596119copy number variation1nstd207human GRCh38 chr10: 6,055,407-6,055,904 , GRCh37.p13 chr10: 6,097,370-6,097,867 IL2RA
    nsv5483953copy number variation1nstd206human GRCh38 chr10: 6,032,210-6,032,292 , GRCh37.p13 chr10: 6,074,173-6,074,255 IL2RA, LOC107984201
    nsv5481919copy number variation1nstd206human GRCh38 chr10: 6,022,807-6,022,878 , GRCh37.p13 chr10: 6,064,770-6,064,841 IL2RA
    nsv5478611copy number variation1nstd206human GRCh38 chr10: 6,055,423-6,055,905 , GRCh37.p13 chr10: 6,097,386-6,097,868 IL2RA
    nsv5393470mobile element deletion2nstd186human GRCh37 chr10: 6,097,386-6,097,868 , GRCh38.p12 chr10: 6,055,423-6,055,905 IL2RA
    nsv5387395copy number variation1nstd186human GRCh37 chr10: 6,064,770-6,064,841 , GRCh38.p12 chr10: 6,022,807-6,022,878 IL2RA
    nsv5339491translocation1nstd200human GRCh37 chr10: 6,064,841-6,064,841 , GRCh37 chr10: 6,064,770-6,064,770 , GRCh38.p12 chr10: 6,022,878-6,022,878 , GRCh38.p12 chr10: 6,022,807-6,022,807 IL2RA
    nsv5325038mobile element deletion1nstd204human GRCh38.p13 chr10: 6,055,423-6,055,905 , GRCh37.p13 chr10: 6,097,386-6,097,868 IL2RA
    nsv5300665copy number variation1nstd204human GRCh38.p13 chr10: 6,022,807-6,022,878 , GRCh37.p13 chr10: 6,064,770-6,064,841 IL2RA
    nsv5133946mobile element insertion1nstd203human GRCh38 chr10: 6,042,148-6,042,168 , GRCh37.p13 chr10: 6,084,111-6,084,131 IL2RA
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