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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5977373copy number variation1nstd209human GRCh38 chrX: 71,205,135-71,215,698 , GRCh37.p13 chrX: 70,424,985-70,435,548 GJB1
    nsv5977131copy number variation2nstd209human GRCh38 chrX: 71,216,744-71,218,789 , GRCh37.p13 chrX: 70,436,594-70,438,639 GJB1
    nsv5976160inversion1nstd209human GRCh38 chrX: 68,979,629-71,845,571 , GRCh37.p13 chrX: 68,199,472-71,065,421 ARR3, DLG3, 73 more genes
    nsv5975831copy number variation2nstd209human GRCh38 chrX: 71,218,086-71,220,636 , GRCh37.p13 chrX: 70,437,936-70,440,486 GJB1
    nsv5974172copy number variation2nstd209human GRCh38 chrX: 71,215,999-71,221,136 , GRCh37.p13 chrX: 70,435,849-70,440,986 GJB1
    nsv5973279copy number variation2nstd209human GRCh38 chrX: 71,212,497-71,220,188 , GRCh37.p13 chrX: 70,432,347-70,440,038 GJB1
    nsv5880738copy number variation1nstd209human GRCh38 chrX: 69,751,799-78,490,154 , GRCh37.p13 chrX: 68,971,643-77,745,651 , MTND4P31, 183 more genes
    nsv5877880copy number variation1nstd209human GRCh38 chrX: 71,215,092-71,220,216 , GRCh37.p13 chrX: 70,434,942-70,440,066 GJB1
    nsv5872369copy number variation1nstd209human GRCh38 chrX: 71,205,614-71,218,783 , GRCh37.p13 chrX: 70,425,464-70,438,633 GJB1
    nsv5728319mobile element insertion2nstd211human GRCh38 chrX: 71,220,164-71,220,164 , GRCh37.p13 chrX: 70,440,014-70,440,014 GJB1
    nsv5717115mobile element insertion2nstd211human GRCh38 chrX: 71,216,209-71,216,209 , GRCh37.p13 chrX: 70,436,059-70,436,059 GJB1
    nsv5619670insertion1nstd207human GRCh38 chrX: 71,220,892-71,220,892 , GRCh37.p13 chrX: 70,440,742-70,440,742 GJB1
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5419112copy number variation1nstd206human GRCh38 chrX: 71,218,784-71,219,544 , GRCh37.p13 chrX: 70,438,634-70,439,394 GJB1
    nsv5418712copy number variation1nstd206human GRCh38 chrX: 71,220,655-71,221,045 , GRCh37.p13 chrX: 70,440,505-70,440,895 GJB1
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5199010mobile element insertion1nstd203human GRCh38 chrX: 71,220,870-71,220,915 , GRCh37.p13 chrX: 70,440,720-70,440,765 GJB1
    nsv5198765mobile element insertion1nstd203human GRCh38 chrX: 71,220,890-71,220,915 , GRCh37.p13 chrX: 70,440,740-70,440,765 GJB1
    nsv5197810mobile element insertion1nstd203human GRCh38 chrX: 71,220,142-71,220,162 , GRCh37.p13 chrX: 70,439,992-70,440,012 GJB1
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