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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048311inversion1nstd229human GRCh38 chr6: 136,780,676-136,782,456 , GRCh37.p13 chr6: 137,101,814-137,103,594 MAP3K5-AS2, MAP3K5
    nsv6816250copy number variation1nstd229human GRCh38 chr6: 136,745,103-136,864,673 , GRCh37.p13 chr6: 137,066,241-137,185,811 PEX7, MAP3K5-AS2, 1 more genes
    nsv6808533copy number variation1nstd229human GRCh38 chr6: 136,766,964-136,829,570 , GRCh37.p13 chr6: 137,088,102-137,150,708 MAP3K5, MAP3K5-AS2, 1 more genes
    nsv6807354copy number variation1nstd229human GRCh38 chr6: 136,437,522-136,955,719 , GRCh37.p13 chr6: 136,758,660-137,276,857 MAP3K5-AS2, RN7SKP299, 8 more genes
    nsv6805748copy number variation1nstd229human GRCh38 chr6: 136,778,999-136,795,794 , GRCh37.p13 chr6: 137,100,137-137,116,932 MAP3K5, MAP3K5-AS2
    nsv6801304copy number variation1nstd229human GRCh38 chr6: 136,782,777-136,784,617 , GRCh37.p13 chr6: 137,103,915-137,105,755 MAP3K5, MAP3K5-AS2
    nsv6314818copy number variation1nstd102humanPathogenic GRCh38 chr6: 134,838,331-142,160,056 , GRCh37.p13 chr6: 135,159,469-142,481,193 PBOV1, IFNGR1, 100 more genes
    nsv6135474copy number variation1nstd213human GRCh37 chr6: 136,910,000-137,260,001 , GRCh38.p12 chr6: 136,588,862-136,938,863 MAP3K5, PEX7, 5 more genes
    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
    nsv5303899copy number variation1nstd204human GRCh38.p13 chr6: 136,677,049-137,315,602 , GRCh37.p13 chr6: 136,998,187-137,636,739 RPL35AP3, LOC105378017, 9 more genes
    nsv5239138copy number variation1nstd204human GRCh38.p13 chr6: 136,676,801-137,315,600 , GRCh37.p13 chr6: 136,997,939-137,636,737 MAP3K5-AS2, NHEG1, 9 more genes
    nsv5105087mobile element insertion1nstd203human GRCh38 chr6: 136,783,385-136,783,395 , GRCh37.p13 chr6: 137,104,523-137,104,533 MAP3K5, MAP3K5-AS2
    nsv4942870copy number variation1nstd200human GRCh38 chr6: 136,782,775-136,784,619 , GRCh37.p13 chr6: 137,103,913-137,105,757 MAP3K5, MAP3K5-AS2
    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
    nsv4612413copy number variation1nstd183human GRCh37 chr6: 137,095,169-137,155,248 , GRCh38.p12 chr6: 136,774,031-136,834,110 PEX7, MAP3K5, 1 more genes
    nsv4488307mobile element insertion1nstd166human GRCh37.p13 chr6: 137,104,523-137,104,523 , GRCh38.p12 chr6: 136,783,385-136,783,385 MAP3K5, MAP3K5-AS2
    nsv4456393copy number variation1nstd102humanUncertain significance GRCh37 chr6: 137,057,372-137,134,336 , GRCh38.p12 chr6: 136,736,234-136,813,198 MAP3K5, MAP3K5-AS2
    nsv4350212copy number variation1nstd102humanPathogenic GRCh37 chr6: 135,239,633-146,997,510 , GRCh38.p12 chr6: 134,918,495-146,676,374 LOC100131041, ADGB-DT, 146 more genes
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