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Items: 1 to 20 of 235

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095677copy number variation1nstd102humanUncertain significance GRCh37 chr19: 8,665,792-8,670,595 , GRCh38.p12 chr19: 8,600,908-8,605,710 ADAMTS10
    nsv7095676copy number variation1nstd102humanUncertain significance GRCh37 chr19: 7,586,521-8,670,595 , GRCh38.p12 chr19: 7,521,635-8,605,710 LRRC8E, ZNF414, 53 more genes
    nsv7095231copy number variation1nstd102humanUncertain significance GRCh37 chr19: 8,645,777-8,662,221 , GRCh38.p12 chr19: 8,580,893-8,597,337 ADAMTS10
    nsv7073704inversion1nstd229human GRCh38 chr19: 8,491,225-8,621,678 , GRCh37.p13 chr19: 8,556,109-8,634,914 ADAMTS10, MYO1F, 2 more genes
    nsv7011964copy number variation1nstd229human GRCh38 chr19: 7,354,369-9,019,195 , GRCh37.p13 chr19: 7,419,271-9,129,871 , MCOLN1, 66 more genes
    nsv7011121copy number variation1nstd229human GRCh38 chr19: 7,159,006-9,938,147 , GRCh37.p13 chr19: 7,159,017-10,048,823 , OR7G1, 117 more genes
    nsv7010144copy number variation1nstd229human GRCh38 chr19: 8,593,027-8,593,587 , GRCh37.p13 chr19: 8,657,911-8,658,471 , GRCh37.p13 chr19|NW_003871094.1: 22,997-23,557 ADAMTS10
    nsv7009716copy number variation1nstd229human GRCh38 chr19: 8,606,477-8,610,591 , GRCh37.p13 chr19|NW_003871094.1: 36,447-40,561 , GRCh37.p13 chr19: 8,671,362-8,675,476 ADAMTS10
    nsv7005936copy number variation1nstd229human GRCh38 chr19: 8,583,079-8,586,645 , GRCh37.p13 chr19|NW_003871094.1: 13,049-16,615 , GRCh37.p13 chr19: 8,647,963-8,651,529 ADAMTS10
    nsv6999385copy number variation1nstd229human GRCh38 chr19: 8,590,733-8,608,083 , GRCh37.p13 chr19|NW_003871094.1: 20,703-38,053 , GRCh37.p13 chr19: 8,655,617-8,672,964 ADAMTS10
    nsv6527673copy number variation1nstd223human GRCh38 chr19: 8,599,443-8,600,746 , GRCh37.p13 chr19: 8,664,327-8,665,630 , GRCh37.p13 chr19|NW_003871094.1: 29,413-30,716 ADAMTS10
    nsv6524417copy number variation1nstd223human GRCh38 chr19: 8,598,827-8,599,727 , GRCh37.p13 chr19|NW_003871094.1: 28,797-29,697 , GRCh37.p13 chr19: 8,663,711-8,664,611 ADAMTS10
    nsv6521117copy number variation1nstd223human GRCh38 chr19: 8,601,506-8,612,609 , GRCh37.p13 chr19: 8,666,390-8,677,494 , GRCh37.p13 chr19|NW_003871094.1: 31,476-42,579 ADAMTS10
    nsv6310653copy number variation1nstd102humanUncertain significance GRCh37 chr19: 8,645,777-8,670,595 , GRCh38.p12 chr19: 8,580,893-8,605,710 ADAMTS10
    nsv6310505copy number variation1nstd102humanPathogenic GRCh37 chr19: 8,656,664-8,670,595 , GRCh38.p12 chr19: 8,591,780-8,605,710 ADAMTS10
    nsv6242779mobile element insertion1nstd215human GRCh38 chr19: 8,592,626-8,592,626 , GRCh37.p13 chr19|NW_003871094.1: 22,596-22,596 , GRCh37.p13 chr19: 8,657,510-8,657,510 ADAMTS10
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
    nsv5974083insertion1nstd209human GRCh38 chr19: 8,581,130-8,581,130 , GRCh37.p13 chr19|NW_003871094.1: 11,100-11,100 , GRCh37.p13 chr19: 8,646,014-8,646,014 ADAMTS10
    nsv5944455copy number variation1nstd209human GRCh38 chr19: 8,598,827-8,599,726 , GRCh37.p13 chr19: 8,663,711-8,664,610 , GRCh37.p13 chr19|NW_003871094.1: 28,797-29,696 ADAMTS10
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