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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112722copy number variation1nstd102humanPathogenic GRCh37 chrX: 42,069,104-45,843,277 , GRCh38.p12 chrX: 42,209,851-45,983,842 TATDN2P1, RRM2P3, 36 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5886182copy number variation1nstd209human GRCh38 chrX: 43,738,206-43,738,290 , GRCh37.p13 chrX: 43,597,453-43,597,537 MAOA
    nsv5885052copy number variation1nstd209human GRCh38 chrX: 43,676,161-43,676,224 , GRCh37.p13 chrX: 43,535,409-43,535,472 MAOA
    nsv5873831copy number variation1nstd209human GRCh38 chrX: 43,657,112-43,657,188 , GRCh37.p13 chrX: 43,516,360-43,516,436 MAOA
    nsv5873682copy number variation1nstd209human GRCh38 chrX: 41,560,623-47,265,899 , GRCh37.p13 chrX: 41,419,876-47,125,298 , CTNNBL1P1, 80 more genes
    nsv5869893copy number variation1nstd209human GRCh38 chrX: 43,718,115-43,718,170 , GRCh37.p13 chrX: 43,577,362-43,577,417 MAOA
    nsv5718681mobile element insertion1nstd211human GRCh38 chrX: 43,713,112-43,713,112 , GRCh37.p13 chrX: 43,572,359-43,572,359 MAOA
    nsv5674214copy number variation1nstd102humanPathogenic GRCh37 chrX: 43,515,570-43,603,780 , GRCh38.p12 chrX: 43,656,322-43,744,533 MAOA
    nsv5614266insertion1nstd207human GRCh38 chrX: 43,713,918-43,713,918 , GRCh37.p13 chrX: 43,573,165-43,573,165 MAOA
    nsv5420555copy number variation1nstd206human GRCh38 chrX: 43,677,763-43,679,108 , GRCh37.p13 chrX: 43,537,011-43,538,356 MAOA
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5415851copy number variation1nstd206human GRCh38 chrX: 43,715,620-43,715,698 , GRCh37.p13 chrX: 43,574,867-43,574,945 MAOA
    nsv5381749copy number variation1nstd102humanPathogenic GRCh37 chrX: 39,645,568-44,199,000 , GRCh38.p12 chrX: 39,786,314-44,339,754 EFHC2, GPR82, 58 more genes
    nsv5381697copy number variation1nstd102humanPathogenic GRCh37 chrX: 41,342,834-43,901,936 , GRCh38.p12 chrX: 41,483,581-44,042,690 GPR82, RNU6-1124P, 22 more genes
    nsv5190052mobile element insertion1nstd203human GRCh38 chrX: 43,706,349-43,706,360 , GRCh37.p13 chrX: 43,565,596-43,565,607 MAOA
    nsv5164961mobile element insertion1nstd203human GRCh38 chrX: 43,740,289-43,740,303 , GRCh37.p13 chrX: 43,599,536-43,599,550 MAOA
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4905436copy number variation1nstd200human GRCh38 chrX: 43,528,401-43,767,159 , GRCh37.p13 chrX: 43,387,649-43,626,406 MAOB, MAOA
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