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Items: 1 to 20 of 248

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077013inversion1nstd229human GRCh38 chr19: 43,341,976-43,391,464 , GRCh37.p13 chr19: 43,846,128-43,895,616 PRG1, TEX101, 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
    nsv7071984inversion1nstd229human GRCh38 chr19: 43,082,679-43,439,776 , GRCh37.p13 chr19: 43,586,831-43,943,928 CD177, PSG5, 13 more genes
    nsv7068669inversion1nstd229human GRCh38 chr19: 43,355,344-43,382,216 , GRCh37.p13 chr19: 43,859,496-43,886,368 CD177, CD177P1
    nsv7067697inversion1nstd229human GRCh38 chr19: 43,355,368-43,405,329 , GRCh37.p13 chr19: 43,859,520-43,909,481 TEX101, LOC110467528, 2 more genes
    nsv7066852inversion1nstd229human GRCh38 chr19: 43,341,123-43,400,200 , GRCh37.p13 chr19: 43,845,275-43,904,352 CD177, CD177P1, 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
    nsv7063321inversion1nstd229human GRCh38 chr19: 43,282,947-43,458,289 , GRCh37.p13 chr19: 43,787,099-43,962,441 PRG1, TEX101, 5 more genes
    nsv7059730inversion1nstd229human GRCh38 chr19: 43,347,399-43,386,155 , GRCh37.p13 chr19: 43,851,551-43,890,307 CD177, CD177P1, 1 more genes
    nsv7014988copy number variation1nstd229human GRCh38 chr19: 43,264,355-43,379,561 , GRCh37.p13 chr19: 43,768,507-43,883,713 PRG1, CEACAMP4, 4 more genes
    nsv7014659copy number variation1nstd229human GRCh38 chr19: 43,348,523-43,351,947 , GRCh37.p13 chr19: 43,852,675-43,856,099 CD177, PRG1
    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
    nsv6635420copy number variation1nstd227human GRCh37 chr19: 43,666,697-43,858,317 , GRCh38.p12 chr19: 43,162,545-43,354,165 , CEACAMP11, 9 more genes
    nsv6625206copy number variation1nstd224human GRCh37 chr19: 43,805,731-43,859,812 , GRCh38.p12 chr19: 43,301,579-43,355,660 CEACAMP4, CD177, 1 more genes
    nsv6625202copy number variation1nstd224human GRCh37 chr19: 43,575,187-43,866,449 , GRCh38.p12 chr19: 43,071,035-43,362,297 CEACAMP10, PSG2, 10 more genes
    nsv6625153copy number variation7nstd224human GRCh37 chr19: 43,805,731-43,858,120 , GRCh38.p12 chr19: 43,301,579-43,353,968 PRG1, CD177, 1 more genes
    nsv6625152copy number variation1nstd224human GRCh37 chr19: 43,754,126-43,857,873 , GRCh38.p12 chr19: 43,249,974-43,353,721 CEACAMP4, PSG9, 3 more genes
    nsv6625146copy number variation1nstd224human GRCh37 chr19: 43,575,187-43,857,873 , GRCh38.p12 chr19: 43,071,035-43,353,721 CEACAMP11, CEACAMP4, 10 more genes
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