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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5938295copy number variation1nstd209human GRCh38 chr19: 13,910,867-13,911,181 , GRCh37.p13 chr19: 14,021,680-14,021,994 CC2D1A
    nsv5709327mobile element insertion1nstd211human GRCh38 chr19: 13,926,057-13,926,057 , GRCh37.p13 chr19: 14,036,870-14,036,870 CC2D1A
    nsv5673147copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 14,023,543-14,032,892 , GRCh38 chr19: 13,912,730-13,922,079 CC2D1A
    nsv5660193insertion1nstd207human GRCh38 chr19: 13,925,946-13,925,946 , GRCh37.p13 chr19: 14,036,759-14,036,759 CC2D1A
    nsv5602593copy number variation1nstd207human GRCh38 chr19: 13,929,745-13,929,834 , GRCh37.p13 chr19: 14,040,558-14,040,647 PODNL1, CC2D1A
    nsv5597205copy number variation1nstd207human GRCh38 chr19: 13,925,932-13,926,027 , GRCh37.p13 chr19: 14,036,745-14,036,840 CC2D1A
    nsv5559736sequence alteration1nstd206human GRCh38 chr19: 13,910,168-13,912,003 , GRCh37.p13 chr19: 14,020,981-14,022,816 CC2D1A
    nsv5531442copy number variation1nstd206human GRCh38 chr19: 13,925,964-13,926,057 , GRCh37.p13 chr19: 14,036,777-14,036,870 CC2D1A
    nsv5524965copy number variation1nstd206human GRCh38 chr19: 13,925,959-13,926,028 , GRCh37.p13 chr19: 14,036,772-14,036,841 CC2D1A
    nsv5514975copy number variation1nstd206human GRCh38 chr19: 13,928,936-13,929,234 , GRCh37.p13 chr19: 14,039,749-14,040,047 CC2D1A, PODNL1
    nsv5300223copy number variation1nstd204human GRCh38.p13 chr19: 13,638,301-14,767,500 , GRCh37.p13 chr19: 13,749,115-14,878,312 , SNORA104, 53 more genes
    nsv5286173copy number variation1nstd204human GRCh38.p13 chr19: 13,764,801-14,012,000 , GRCh37.p13 chr19: 13,875,615-14,122,812 , MIR181C, 16 more genes
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv4657127copy number variation2nstd186human GRCh37 chr19: 14,036,772-14,036,841 , GRCh38.p12 chr19: 13,925,959-13,926,028 CC2D1A
    nsv4555073insertion1nstd166human GRCh37.p13 chr19: 14,036,759-14,036,759 , GRCh38.p12 chr19: 13,925,946-13,925,946 CC2D1A
    nsv4552878insertion1nstd166human GRCh37.p13 chr19: 14,036,789-14,036,789 , GRCh38.p12 chr19: 13,925,976-13,925,976 CC2D1A
    nsv4264929copy number variation1nstd166human GRCh37.p13 chr19: 14,029,416-14,029,474 , GRCh38.p12 chr19: 13,918,603-13,918,661 CC2D1A
    nsv4260955copy number variation1nstd166human GRCh37.p13 chr19: 14,036,535-14,036,711 , GRCh38.p12 chr19: 13,925,722-13,925,898 CC2D1A
    nsv4257198copy number variation1nstd166human GRCh37.p13 chr19: 14,036,772-14,036,841 , GRCh38.p12 chr19: 13,925,959-13,926,028 CC2D1A
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