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Items: 1 to 20 of 150

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095657copy number variation1nstd102humanUncertain significance GRCh37 chr19: 44,011,002-45,213,778 , GRCh38.p12 chr19: 43,506,850-44,710,506 RN7SL368P, ZNF112, 52 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
    nsv7066709inversion1nstd229human GRCh38 chr19: 40,109,835-46,893,669 , GRCh37.p13 chr19: 40,615,742-47,396,926 LOC105372405, RNU6-611P, 305 more genes
    nsv7066137inversion1nstd229human GRCh38 chr19: 43,668,049-45,225,177 , GRCh37.p13 chr19: 44,172,201-45,728,435 LOC107985306, LYPD5, 67 more genes
    nsv7061070inversion1nstd229human GRCh38 chr19: 43,830,632-43,949,861 , GRCh37.p13 chr19: 44,334,784-44,454,013 ZNF45, ZNF221, 3 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
    nsv7011402copy number variation1nstd229human GRCh38 chr19: 43,942,230-43,954,124 , GRCh37.p13 chr19: 44,446,382-44,458,276 ZNF221
    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
    nsv7007881copy number variation1nstd229human GRCh38 chr19: 43,905,240-43,987,894 , GRCh37.p13 chr19: 44,409,392-44,492,046 ZNF221, ZNF45, 1 more genes
    nsv6625017copy number variation1nstd224human GRCh37 chr19: 44,446,850-44,471,212 , GRCh38.p12 chr19: 43,942,698-43,967,060 ZNF155, ZNF221
    nsv6625016copy number variation1nstd224human GRCh37 chr19: 44,446,850-44,471,125 , GRCh38.p12 chr19: 43,942,698-43,966,973 ZNF155, ZNF221
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 more genes
    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
    nsv5525244copy number variation1nstd206human GRCh38 chr19: 43,951,851-43,952,172 , GRCh37.p13 chr19: 44,456,003-44,456,324 ZNF221
    nsv5207086mobile element deletion1nstd204human GRCh38.p13 chr19: 43,951,844-43,952,177 , GRCh37.p13 chr19: 44,455,996-44,456,329 ZNF221
    nsv5020614copy number variation1nstd200human GRCh38 chr19: 43,905,240-43,987,892 , GRCh37.p13 chr19: 44,409,392-44,492,044 ZNF221, ZNF45, 1 more genes
    nsv4907546mobile element deletion1nstd200human GRCh38 chr19: 43,951,850-43,952,172 , GRCh37.p13 chr19: 44,456,002-44,456,324 ZNF221
    nsv4868518copy number variation1nstd200human GRCh37 chr19: 44,409,392-44,492,044 , GRCh38.p12 chr19: 43,905,240-43,987,892 ZNF221, ZNF45, 1 more genes
    nsv4775418mobile element deletion1nstd200human GRCh37 chr19: 44,456,003-44,456,324 , GRCh38.p12 chr19: 43,951,851-43,952,172 ZNF221
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