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Items: 1 to 20 of 293

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112726copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,810,210-140,046,615 , GRCh38.p12 chr6: 133,489,072-139,725,478 SIMALR, MTFR2, 99 more genes
    nsv5905770copy number variation1nstd209human GRCh38 chr6: 136,284,094-136,284,143 , GRCh37.p13 chr6: 136,605,232-136,605,281 BCLAF1
    nsv5344557translocation1nstd200human GRCh37 chr6: 136,603,827-136,603,827 , GRCh37 chr6: 136,610,849-136,610,849 , GRCh38.p12 chr6: 136,289,711-136,289,711 , GRCh38.p12 chr6: 136,282,689-136,282,689 BCLAF1
    nsv5335434translocation1nstd200human GRCh37 chr6: 136,582,615-136,582,615 , GRCh37 chr6: 136,589,299-136,589,299 , GRCh38.p12 chr6: 136,261,477-136,261,477 , GRCh38.p12 chr6: 136,268,161-136,268,161 BCLAF1
    nsv4716273copy number variation4nstd195human GRCh37 chr6: 136,597,644-136,597,645 , GRCh38.p12 chr6: 136,276,506-136,276,507 BCLAF1
    nsv4712273copy number variation1nstd195human GRCh37 chr6: 136,599,906-136,599,907 , GRCh38.p12 chr6: 136,278,768-136,278,769 BCLAF1
    nsv4711783translocation1nstd195human GRCh37 chr5: 110,284,665-110,284,665 , GRCh37 chr6: 136,596,980-136,596,980 , GRCh38.p12 chr5: 110,948,966-110,948,966 , GRCh38.p12 chr6: 136,275,842-136,275,842 BCLAF1, BCLAF1P1
    nsv4711439translocation1nstd195human GRCh37 chr5: 110,284,665-110,284,665 , GRCh37 chr6: 136,596,981-136,596,981 , GRCh38.p12 chr5: 110,948,966-110,948,966 , GRCh38.p12 chr6: 136,275,843-136,275,843 BCLAF1, BCLAF1P1
    nsv4710791copy number variation2nstd195human GRCh37 chr6: 136,582,615-136,582,616 , GRCh38.p12 chr6: 136,261,477-136,261,478 BCLAF1
    nsv4710622copy number variation1nstd195human GRCh37 chr6: 136,589,477-136,589,478 , GRCh38.p12 chr6: 136,268,339-136,268,340 BCLAF1
    nsv4710245translocation1nstd195human GRCh37 chr5: 110,286,524-110,286,524 , GRCh37 chr6: 136,599,910-136,599,910 , GRCh38.p12 chr5: 110,950,825-110,950,825 , GRCh38.p12 chr6: 136,278,772-136,278,772 BCLAF1, BCLAF1P1
    nsv4708312translocation1nstd195human GRCh37 chr5: 110,286,524-110,286,524 , GRCh37 chr6: 136,599,911-136,599,911 , GRCh38.p12 chr5: 110,950,825-110,950,825 , GRCh38.p12 chr6: 136,278,773-136,278,773 BCLAF1, BCLAF1P1
    nsv4708012translocation1nstd195human GRCh37 chr5: 110,285,598-110,285,598 , GRCh37 chr6: 136,599,000-136,599,000 , GRCh38.p12 chr5: 110,949,899-110,949,899 , GRCh38.p12 chr6: 136,277,862-136,277,862 BCLAF1, BCLAF1P1
    nsv4705488copy number variation1nstd195human GRCh37 chr6: 136,593,216-136,593,217 , GRCh38.p12 chr6: 136,272,078-136,272,079 BCLAF1
    nsv4705055translocation1nstd195human GRCh37 chr5: 110,285,598-110,285,598 , GRCh37 chr6: 136,599,001-136,599,001 , GRCh38.p12 chr5: 110,949,899-110,949,899 , GRCh38.p12 chr6: 136,277,863-136,277,863 BCLAF1, BCLAF1P1
    nsv4685709copy number variation1nstd102humannot provided GRCh37 chr6: 135,936,688-140,660,269 , GRCh38.p12 chr6: 135,615,550-140,339,132 MAP7, RN7SKP299, 74 more genes
    nsv4683010copy number variation1nstd102humanPathogenic GRCh37 chr6: 136,482,728-137,540,520 , GRCh38.p12 chr6: 136,161,590-137,219,383 PDE7B, RN7SKP299, 17 more genes
    nsv4675250copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,817,341-140,038,401 , GRCh38.p12 chr6: 133,496,203-139,717,264 ALDH8A1, IL22RA2, 99 more genes
    nsv4616259copy number variation1nstd183human GRCh37 chr6: 136,582,615-136,589,299 , GRCh38.p12 chr6: 136,261,477-136,268,161 BCLAF1
    nsv4487703mobile element insertion1nstd166human GRCh37.p13 chr6: 136,580,960-136,580,960 , GRCh38.p12 chr6: 136,259,822-136,259,822 BCLAF1
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