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Items: 1 to 20 of 102

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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
    nsv6999250copy number variation1nstd229human GRCh38 chr19: 43,599,599-43,600,056 , GRCh37.p13 chr19: 44,103,751-44,104,208 ZNF576
    nsv6598416inversion1nstd223human GRCh38 chr19: 40,109,815-44,449,696 , GRCh37.p13 chr19: 40,615,722-44,953,884 , SERTAD1, 188 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
    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
    nsv5928300copy number variation1nstd209human GRCh38 chr19: 43,601,565-43,601,639 , GRCh37.p13 chr19: 44,105,717-44,105,791 ZNF576
    nsv5024695copy number variation1nstd200human GRCh38 chr19: 43,599,599-43,600,058 , GRCh37.p13 chr19: 44,103,751-44,104,210 ZNF576
    nsv5020599copy number variation1nstd200human GRCh38 chr19: 43,596,792-43,596,964 , GRCh37.p13 chr19: 44,100,944-44,101,116 ZNF576
    nsv4868506copy number variation1nstd200human GRCh37 chr19: 44,105,717-44,105,793 , GRCh38.p12 chr19: 43,601,565-43,601,641 ZNF576
    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
    nsv4457468copy number variation1nstd102humanUncertain significance GRCh37 chr19: 43,818,072-44,100,076 , GRCh38.p12 chr19: 43,313,920-43,595,924 CD177, LYPD3, 11 more genes
    nsv4457412copy number variation1nstd102humanUncertain significance GRCh37 chr19: 43,803,157-44,105,375 , GRCh38.p12 chr19: 43,299,005-43,601,223 ZNF575, CEACAMP4, 12 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4270741copy number variation1nstd166human GRCh37.p13 chr19: 44,090,567-44,105,700 , GRCh38.p12 chr19: 43,586,415-43,601,548 ZNF576, IRGQ
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