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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970603inversion1nstd209human GRCh38 chr9: 122,761,784-123,114,887 , GRCh37.p13 chr9: 125,524,063-125,877,166 GPR21, PDCL, 16 more genes
    nsv5925623copy number variation1nstd209human GRCh38 chr9: 122,867,212-122,867,309 , GRCh37.p13 chr9: 125,629,491-125,629,588 RC3H2
    nsv5909122copy number variation1nstd209human GRCh38 chr9: 122,820,722-122,861,228 , GRCh37.p13 chr9: 125,583,001-125,623,507 KRT18P67, PDCL, 1 more genes
    nsv5867123copy number variation1nstd209human GRCh38 chr9: 122,839,674-122,844,723 , GRCh37.p13 chr9: 125,601,953-125,607,002 RC3H2
    nsv5865769copy number variation1nstd209human GRCh38 chr9: 122,839,624-122,843,223 , GRCh37.p13 chr9: 125,601,903-125,605,502 RC3H2
    nsv5864551copy number variation1nstd209human GRCh38 chr9: 122,847,866-122,851,320 , GRCh37.p13 chr9: 125,610,145-125,613,599 RC3H2
    nsv5860010copy number variation1nstd209human GRCh38 chr9: 122,853,987-122,858,436 , GRCh37.p13 chr9: 125,616,266-125,620,715 RC3H2
    nsv5859222copy number variation1nstd209human GRCh38 chr9: 122,845,224-122,847,615 , GRCh37.p13 chr9: 125,607,503-125,609,894 RC3H2
    nsv5856810copy number variation1nstd209human GRCh38 chr9: 122,853,637-122,861,736 , GRCh37.p13 chr9: 125,615,916-125,624,015 RC3H2
    nsv5847870copy number variation1nstd209human GRCh38 chr9: 122,855,937-122,861,436 , GRCh37.p13 chr9: 125,618,216-125,623,715 RC3H2
    nsv5706935mobile element insertion1nstd211human GRCh38 chr9: 122,865,765-122,865,765 , GRCh37.p13 chr9: 125,628,044-125,628,044 RC3H2
    nsv5700460mobile element insertion1nstd211human GRCh38 chr9: 122,870,408-122,870,408 , GRCh37.p13 chr9: 125,632,687-125,632,687 RC3H2
    nsv5628199insertion1nstd207human GRCh38 chr9: 122,867,905-122,867,905 , GRCh37.p13 chr9: 125,630,184-125,630,184 RC3H2
    nsv5626877insertion1nstd207human GRCh38 chr9: 122,867,261-122,867,261 , GRCh37.p13 chr9: 125,629,540-125,629,540 RC3H2
    nsv5624888insertion1nstd207human GRCh38 chr9: 122,866,857-122,866,857 , GRCh37.p13 chr9: 125,629,136-125,629,136 RC3H2
    nsv5589088copy number variation1nstd207human GRCh38 chr9: 122,866,857-122,867,517 , GRCh37.p13 chr9: 125,629,136-125,629,796 RC3H2
    nsv5588377copy number variation1nstd207human GRCh38 chr9: 122,867,827-122,867,915 , GRCh37.p13 chr9: 125,630,106-125,630,194 RC3H2
    nsv5402108mobile element insertion1nstd206human GRCh38 chr9: 122,865,765-122,865,816 , GRCh37.p13 chr9: 125,628,044-125,628,095 RC3H2
    nsv5199158mobile element insertion1nstd203human GRCh38 chr9: 122,868,872-122,868,872 , GRCh37.p13 chr9: 125,631,151-125,631,151 RC3H2
    nsv5197340mobile element insertion1nstd203human GRCh38 chr9: 122,868,864-122,868,864 , GRCh37.p13 chr9: 125,631,143-125,631,143 RC3H2
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