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Items: 1 to 20 of 128

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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
    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
    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
    nsv6625155copy number variation1nstd224human GRCh37 chr19: 43,885,085-43,964,028 , GRCh38.p12 chr19: 43,380,933-43,459,876 LYPD3, TEX101, 1 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
    nsv6530649copy number variation1nstd223human GRCh38 chr19: 42,576,896-43,593,497 , GRCh37.p13 chr19: 43,081,048-44,097,649 , PSG3, 37 more genes
    nsv6314086copy number variation1nstd102humanUncertain significance GRCh37 chr19: 43,082,847-44,100,076 , GRCh38.p12 chr19: 42,578,695-43,595,924 PSG9, PSG8-AS1, 37 more genes
    nsv6251063mobile element insertion1nstd215human GRCh38 chr19: 43,462,116-43,462,116 , GRCh37.p13 chr19: 43,966,268-43,966,268 LYPD3
    nsv6133703copy number variation1nstd213human GRCh37 chr19: 41,220,000-49,640,001 , GRCh38.p12 chr19: 40,714,095-49,136,744 , APOC1, 402 more genes
    nsv6133474copy number variation1nstd213human GRCh37 chr19: 42,350,000-49,650,001 , GRCh38.p12 chr19: 41,845,937-49,146,744 , APOC1, 343 more genes
    nsv5525802copy number variation1nstd206human GRCh38 chr19: 43,378,874-43,458,874 , GRCh37.p13 chr19: 43,883,026-43,963,026 LYPD3, TEX101, 2 more genes
    nsv5024672copy number variation1nstd200human GRCh38 chr19: 42,797,406-43,578,600 , GRCh37.p13 chr19: 43,301,558-44,082,752 , PINLYP, 28 more genes
    nsv5020588copy number variation1nstd200human GRCh38 chr19: 43,464,594-43,464,708 , GRCh37.p13 chr19: 43,968,746-43,968,860 LYPD3
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