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Items: 1 to 20 of 338

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925655copy number variation1nstd209human GRCh38 chr11: 1,286,639-1,286,693 , GRCh37.p13 chr11: 1,307,869-1,307,923 TOLLIP
    nsv5919456copy number variation1nstd209human GRCh38 chr11: 1,289,752-1,289,822 , GRCh37.p13 chr11: 1,310,982-1,311,052 TOLLIP
    nsv5918738copy number variation1nstd209human GRCh38 chr11: 736,859-3,895,958 , GRCh37.p13 chr11: 736,859-3,917,188 , TALDO1, 128 more genes
    nsv5917762copy number variation1nstd209human GRCh38 chr11: 1,286,730-1,286,827 , GRCh37.p13 chr11: 1,307,960-1,308,057 TOLLIP
    nsv5707878mobile element insertion1nstd211human GRCh38 chr11: 1,303,174-1,303,174 , GRCh37.p13 chr11: 1,324,404-1,324,404 TOLLIP
    nsv5663912insertion1nstd207human GRCh38 chr11: 1,294,476-1,294,476 , GRCh37.p13 chr11: 1,315,706-1,315,706 TOLLIP
    nsv5663022insertion1nstd207human GRCh38 chr11: 1,287,422-1,287,422 , GRCh37.p13 chr11: 1,308,652-1,308,652 TOLLIP
    nsv5662621insertion1nstd207human GRCh38 chr11: 1,287,808-1,287,808 , GRCh37.p13 chr11: 1,309,038-1,309,038 TOLLIP
    nsv5659271insertion1nstd207human GRCh38 chr11: 1,287,794-1,287,794 , GRCh37.p13 chr11: 1,309,024-1,309,024 TOLLIP
    nsv5658653insertion1nstd207human GRCh38 chr11: 1,294,833-1,294,833 , GRCh37.p13 chr11: 1,316,063-1,316,063 TOLLIP
    nsv5658428insertion2nstd207human GRCh38 chr11: 1,287,836-1,287,836 , GRCh37.p13 chr11: 1,309,066-1,309,066 TOLLIP
    nsv5655493insertion1nstd207human GRCh38 chr11: 1,294,739-1,294,739 , GRCh37.p13 chr11: 1,315,969-1,315,969 TOLLIP
    nsv5652809insertion1nstd207human GRCh38 chr11: 1,294,490-1,294,490 , GRCh37.p13 chr11: 1,315,720-1,315,720 TOLLIP
    nsv5648322insertion1nstd207human GRCh38 chr11: 1,287,514-1,287,514 , GRCh37.p13 chr11: 1,308,744-1,308,744 TOLLIP
    nsv5645368insertion1nstd207human GRCh38 chr11: 1,294,201-1,294,201 , GRCh37.p13 chr11: 1,315,431-1,315,431 TOLLIP
    nsv5644663insertion1nstd207human GRCh38 chr11: 1,287,479-1,287,479 , GRCh37.p13 chr11: 1,308,709-1,308,709 TOLLIP
    nsv5603339copy number variation1nstd207human GRCh38 chr11: 1,294,762-1,294,902 , GRCh37.p13 chr11: 1,315,992-1,316,132 TOLLIP
    nsv5602155copy number variation1nstd207human GRCh38 chr11: 1,294,490-1,294,912 , GRCh37.p13 chr11: 1,315,720-1,316,142 TOLLIP
    nsv5594861copy number variation1nstd207human GRCh38 chr11: 1,294,348-1,294,440 , GRCh37.p13 chr11: 1,315,578-1,315,670 TOLLIP
    nsv5592834copy number variation1nstd207human GRCh38 chr11: 1,296,813-1,296,868 , GRCh37.p13 chr11: 1,318,043-1,318,098 , TOLLIP
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