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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921935copy number variation1nstd209human GRCh38 chr9: 5,304,739-5,339,884 , GRCh37.p13 chr9: 5,304,739-5,339,884 RLN1, RLN2, 1 more genes
    nsv5915802copy number variation1nstd209human GRCh38 chr9: 4,956,818-6,213,781 , GRCh37.p13 chr9: 4,956,818-6,213,781 , RLN1, 30 more genes
    nsv5913722copy number variation1nstd209human GRCh38 chr9: 5,318,865-5,339,588 , GRCh37.p13 chr9: 5,318,865-5,339,588 RLN2, RLN1
    nsv5865126copy number variation2nstd209human GRCh38 chr9: 5,302,707-5,318,916 , GRCh37.p13 chr9: 5,302,707-5,318,916 RLN1, RLN2, 1 more genes
    nsv5864744copy number variation2nstd209human GRCh38 chr9: 5,310,925-5,318,612 , GRCh37.p13 chr9: 5,310,925-5,318,612 RLN2, RLN1, 1 more genes
    nsv5856439copy number variation2nstd209human GRCh38 chr9: 5,316,325-5,330,787 , GRCh37.p13 chr9: 5,316,325-5,330,787 RLN1, RLN2
    nsv5855547copy number variation2nstd209human GRCh38 chr9: 5,330,288-5,337,321 , GRCh37.p13 chr9: 5,330,288-5,337,321 RLN1, RLN2
    nsv5854055copy number variation2nstd209human GRCh38 chr9: 5,323,710-5,331,959 , GRCh37.p13 chr9: 5,323,710-5,331,959 RLN2, RLN1
    nsv5708210mobile element insertion1nstd211human GRCh38 chr9: 5,307,954-5,307,954 , GRCh37.p13 chr9: 5,307,954-5,307,954 RLN1, RLN2
    nsv5700829mobile element insertion2nstd211human GRCh38 chr9: 5,330,782-5,330,782 , GRCh37.p13 chr9: 5,330,782-5,330,782 RLN2, RLN1
    nsv5492926copy number variation1nstd206human GRCh38 chr9: 5,304,000-5,339,000 , GRCh37.p13 chr9: 5,304,000-5,339,000 RLN1, RLN2, 1 more genes
    nsv5486860copy number variation1nstd206human GRCh38 chr9: 5,318,869-5,339,589 , GRCh37.p13 chr9: 5,318,869-5,339,589 RLN2, RLN1
    nsv5476530copy number variation1nstd206human GRCh38 chr9: 5,320,960-5,396,852 , GRCh37.p13 chr9: 5,320,960-5,396,852 PLGRKT, RLN1, 1 more genes
    nsv5476490copy number variation1nstd206human GRCh38 chr9: 5,314,945-5,315,027 , GRCh37.p13 chr9: 5,314,945-5,315,027 RLN1, RLN2
    nsv5408897mobile element insertion1nstd206human GRCh38 chr9: 5,307,954-5,308,005 , GRCh37.p13 chr9: 5,307,954-5,308,005 RLN1, RLN2
    nsv5381785copy number variation1nstd102humanPathogenic GRCh37 chr9: 2,854,435-6,937,677 , GRCh38.p12 chr9: 2,854,435-6,937,677 GLIS3-AS1, RFX3-DT, 70 more genes
    nsv5381767copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814 ACTG1P14, DMAC1, 191 more genes
    nsv5381702copy number variation1nstd102humanUncertain significance GRCh37 chr9: 2,029,023-5,300,444 , GRCh38.p12 chr9: 2,029,023-5,300,444 MTND5P36, MTND2P36, 53 more genes
    nsv5372214translocation1nstd200human GRCh38 chr9: 5,300,273-5,300,273 , GRCh38 chr9: 5,335,316-5,335,316 , GRCh37.p13 chr9: 5,335,316-5,335,316 , GRCh37.p13 chr9: 5,300,273-5,300,273 RLN2, RLN1
    nsv5364592translocation1nstd200human GRCh38 chr9: 5,329,550-5,329,550 , GRCh38 chr9: 5,329,617-5,329,617 , GRCh37.p13 chr9: 5,329,550-5,329,550 , GRCh37.p13 chr9: 5,329,617-5,329,617 RLN2, RLN1
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