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Items: 1 to 20 of 269

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077675inversion1nstd229human GRCh38 chr19: 43,438,575-43,535,950 , GRCh37.p13 chr19: 43,942,727-44,040,102 ETHE1, LYPD3, 2 more genes
    nsv7074377inversion1nstd229human GRCh38 chr19: 41,965,396-49,981,454 , GRCh37.p13 chr19: 42,514,712-50,484,711 IGFL1, SYMPK, 400 more genes
    nsv7073743inversion1nstd229human GRCh38 chr19: 43,451,045-43,551,151 , GRCh37.p13 chr19: 43,955,197-44,055,303 XRCC1, ZNF575, 3 more genes
    nsv7072490inversion1nstd229human GRCh38 chr19: 43,438,672-43,536,045 , GRCh37.p13 chr19: 43,942,824-44,040,197 ZNF575, PHLDB3, 2 more genes
    nsv7066709inversion1nstd229human GRCh38 chr19: 40,109,835-46,893,669 , GRCh37.p13 chr19: 40,615,742-47,396,926 LOC105372405, RNU6-611P, 305 more genes
    nsv7059316inversion1nstd229human GRCh38 chr19: 43,396,877-48,200,638 , GRCh37.p13 chr19: 43,901,029-48,703,895 GEMIN7, ZNF229, 212 more genes
    nsv7009973copy number variation1nstd229human GRCh38 chr19: 43,265,923-43,495,049 , GRCh37.p13 chr19: 43,770,075-43,999,201 CEACAMP11, PSG9, 8 more genes
    nsv7008844copy number variation1nstd229human GRCh38 chr19: 43,479,397-43,482,966 , GRCh37.p13 chr19: 43,983,549-43,987,118 PHLDB3
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7005491copy number variation1nstd229human GRCh38 chr19: 43,471,796-43,487,312 , GRCh37.p13 chr19: 43,975,948-43,991,464 PHLDB3
    nsv7004565copy number variation1nstd229human GRCh38 chr19: 43,481,474-43,500,003 , GRCh37.p13 chr19: 43,985,626-44,004,155 PHLDB3
    nsv7001254copy number variation1nstd229human GRCh38 chr19: 43,496,565-43,530,952 , GRCh37.p13 chr19: 44,000,717-44,035,104 ZNF575, PHLDB3, 1 more genes
    nsv6999910copy number variation1nstd229human GRCh38 chr19: 43,484,276-43,487,256 , GRCh37.p13 chr19: 43,988,428-43,991,408 PHLDB3
    nsv6999646copy number variation1nstd229human GRCh38 chr19: 43,481,433-43,500,109 , GRCh37.p13 chr19: 43,985,585-44,004,261 PHLDB3
    nsv6999542copy number variation1nstd229human GRCh38 chr19: 43,477,235-43,477,823 , GRCh37.p13 chr19: 43,981,387-43,981,975 PHLDB3
    nsv6998798copy number variation1nstd229human GRCh38 chr19: 43,469,996-43,484,618 , GRCh37.p13 chr19: 43,974,148-43,988,770 PHLDB3
    nsv6998502copy number variation1nstd229human GRCh38 chr19: 43,478,001-43,483,400 , GRCh37.p13 chr19: 43,982,153-43,987,552 PHLDB3
    nsv6637474copy number variation1nstd102humanUncertain significance GRCh37 chr19: 43,084,067-44,096,910 , GRCh38.p12 chr19: 42,579,915-43,592,758 CEACAMP10, PRG1, 36 more genes
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 more genes
    nsv6533267copy number variation1nstd223human GRCh38 chr19: 42,797,480-43,578,160 , GRCh37.p13 chr19: 43,301,632-44,082,312 , PSG1, 28 more genes
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