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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
    nsv7059316inversion1nstd229human GRCh38 chr19: 43,396,877-48,200,638 , GRCh37.p13 chr19: 43,901,029-48,703,895 GEMIN7, ZNF229, 212 more genes
    nsv7014737copy number variation1nstd229human GRCh38 chr19: 43,559,820-43,683,290 , GRCh37.p13 chr19: 44,063,972-44,187,442 RN7SL368P, PLAUR, 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
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 more genes
    nsv6251064mobile element insertion1nstd215human GRCh38 chr19: 43,610,545-43,610,545 , GRCh37.p13 chr19: 44,114,697-44,114,697 SRRM5, ZNF428
    nsv6226583copy number variation1nstd214human GRCh38 chr19: 43,613,358-43,613,429 , GRCh37.p13 chr19: 44,117,510-44,117,581 SRRM5, ZNF428
    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
    nsv5971810insertion1nstd209human GRCh38 chr19: 43,610,531-43,610,531 , GRCh37.p13 chr19: 44,114,683-44,114,683 SRRM5, ZNF428
    nsv5945957copy number variation1nstd209human GRCh38 chr19: 43,613,592-43,613,663 , GRCh37.p13 chr19: 44,117,744-44,117,815 SRRM5, ZNF428
    nsv5712568mobile element insertion2nstd211human GRCh38 chr19: 43,610,545-43,610,545 , GRCh37.p13 chr19: 44,114,697-44,114,697 ZNF428, SRRM5
    nsv5653574insertion1nstd207human GRCh38 chr19: 43,610,531-43,610,531 , GRCh37.p13 chr19: 44,114,683-44,114,683 SRRM5, ZNF428
    nsv5419881mobile element insertion1nstd206human GRCh38 chr19: 43,610,545-43,610,578 , GRCh37.p13 chr19: 44,114,697-44,114,730 ZNF428, SRRM5
    nsv5179648mobile element insertion1nstd203human GRCh38 chr19: 43,610,536-43,610,545 , GRCh37.p13 chr19: 44,114,688-44,114,697 SRRM5, ZNF428
    nsv5165903mobile element insertion1nstd203human GRCh38 chr19: 43,610,531-43,610,545 , GRCh37.p13 chr19: 44,114,683-44,114,697 ZNF428, SRRM5
    nsv4679272copy number variation1nstd189human GRCh37.p13 chr19: 43,906,705-44,198,705 , GRCh38.p12 chr19: 43,402,553-43,694,553 , PLAUR, 16 more genes
    nsv4504935mobile element insertion1nstd166human GRCh37.p13 chr19: 44,114,683-44,114,683 , GRCh38.p12 chr19: 43,610,531-43,610,531 ZNF428, SRRM5
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