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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5957589insertion1nstd209human GRCh38 chr9: 83,693,775-83,693,775 , GRCh37.p13 chr9: 86,308,690-86,308,690 UBQLN1
    nsv5908389copy number variation1nstd209human GRCh38 chr9: 83,671,423-83,671,649 , GRCh37.p13 chr9: 86,286,338-86,286,564 UBQLN1
    nsv5721891mobile element insertion1nstd211human GRCh38 chr9: 83,699,043-83,699,043 , GRCh37.p13 chr9: 86,313,958-86,313,958 UBQLN1
    nsv5707230mobile element insertion2nstd211human GRCh38 chr9: 83,693,791-83,693,791 , GRCh37.p13 chr9: 86,308,706-86,308,706 UBQLN1
    nsv5706941mobile element insertion1nstd211human GRCh38 chr9: 83,670,375-83,670,375 , GRCh37.p13 chr9: 86,285,290-86,285,290 UBQLN1
    nsv5702612mobile element insertion2nstd211human GRCh38 chr9: 83,681,090-83,681,090 , GRCh37.p13 chr9: 86,296,005-86,296,005 UBQLN1
    nsv5535888insertion1nstd206human GRCh38 chr9: 83,681,090-83,681,133 , GRCh37.p13 chr9: 86,296,005-86,296,048 UBQLN1
    nsv5480972copy number variation1nstd206human GRCh38 chr9: 83,671,426-83,671,650 , GRCh37.p13 chr9: 86,286,341-86,286,565 UBQLN1
    nsv5474877copy number variation1nstd206human GRCh38 chr9: 83,683,180-83,683,751 , GRCh37.p13 chr9: 86,298,095-86,298,666 UBQLN1
    nsv5410228mobile element insertion1nstd206human GRCh38 chr9: 83,693,791-83,693,842 , GRCh37.p13 chr9: 86,308,706-86,308,757 UBQLN1
    nsv5400668mobile element insertion1nstd206human GRCh38 chr9: 83,670,375-83,670,382 , GRCh37.p13 chr9: 86,285,290-86,285,297 UBQLN1
    nsv5399877mobile element insertion1nstd206human GRCh38 chr9: 83,677,185-83,677,236 , GRCh37.p13 chr9: 86,292,100-86,292,151 UBQLN1
    nsv5372711translocation1nstd200human GRCh38 chr9: 83,699,901-83,699,901 , GRCh38 chr9: 83,699,967-83,699,967 , GRCh37.p13 chr9: 86,314,816-86,314,816 , GRCh37.p13 chr9: 86,314,882-86,314,882 UBQLN1
    nsv5372710translocation1nstd200human GRCh38 chr9: 83,683,179-83,683,179 , GRCh38 chr9: 83,683,749-83,683,749 , GRCh37.p13 chr9: 86,298,094-86,298,094 , GRCh37.p13 chr9: 86,298,664-86,298,664 UBQLN1
    nsv5372709translocation1nstd200human GRCh38 chr9: 83,671,650-83,671,650 , GRCh38 chr9: 83,671,426-83,671,426 , GRCh37.p13 chr9: 86,286,565-86,286,565 , GRCh37.p13 chr9: 86,286,341-86,286,341 UBQLN1
    nsv5332460translocation1nstd200human GRCh37 chr9: 86,314,882-86,314,882 , GRCh37 chr9: 86,314,816-86,314,816 , GRCh38.p12 chr9: 83,699,967-83,699,967 , GRCh38.p12 chr9: 83,699,901-83,699,901 UBQLN1
    nsv5319889copy number variation1nstd204human GRCh38.p13 chr9: 83,683,156-83,683,772 , GRCh37.p13 chr9: 86,298,071-86,298,687 UBQLN1
    nsv5127929mobile element insertion1nstd203human GRCh38 chr9: 83,692,940-83,692,952 , GRCh37.p13 chr9: 86,307,855-86,307,867 UBQLN1
    nsv5036269inversion1nstd200human GRCh38 chr9: 79,108,237-87,224,469 , GRCh37.p13 chr9: 81,723,153-89,839,384 , RMI1, 100 more genes
    nsv4953047copy number variation1nstd200human GRCh38 chr9: 83,704,771-83,707,258 , GRCh37.p13 chr9: 86,319,686-86,322,173 UBQLN1-AS1, UBQLN1
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