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Items: 1 to 20 of 237

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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
    nsv5968494inversion1nstd209human GRCh38 chr6: 125,606,968-134,343,905 , GRCh37.p13 chr6: 125,928,114-134,665,043 , ARG1, 137 more genes
    nsv5959255insertion1nstd209human GRCh38 chr6: 133,987,647-133,987,647 , GRCh37.p13 chr6: 134,308,785-134,308,785 SLC2A12, TBPL1
    nsv5902710copy number variation1nstd209human GRCh38 chr6: 134,032,405-134,032,470 , GRCh37.p13 chr6: 134,353,543-134,353,608 SLC2A12
    nsv5844380copy number variation1nstd209human GRCh38 chr6: 134,030,750-134,032,099 , GRCh37.p13 chr6: 134,351,888-134,353,237 SLC2A12
    nsv5685902mobile element insertion2nstd211human GRCh38 chr6: 133,990,918-133,990,918 , GRCh37.p13 chr6: 134,312,056-134,312,056 SLC2A12, TBPL1
    nsv5681738mobile element insertion1nstd211human GRCh38 chr6: 134,038,726-134,038,726 , GRCh37.p13 chr6: 134,359,864-134,359,864 SLC2A12
    nsv5580123copy number variation1nstd207human GRCh38 chr6: 134,032,405-134,032,470 , GRCh37.p13 chr6: 134,353,543-134,353,608 SLC2A12
    nsv5469338copy number variation1nstd206human GRCh38 chr6: 134,032,421-134,032,471 , GRCh37.p13 chr6: 134,353,559-134,353,609 SLC2A12
    nsv5467293copy number variation1nstd206human GRCh38 chr6: 133,984,239-133,986,506 , GRCh37.p13 chr6: 134,305,377-134,307,644 TBPL1, SLC2A12
    nsv5465533copy number variation1nstd206human GRCh38 chr6: 134,030,768-134,033,135 , GRCh37.p13 chr6: 134,351,906-134,354,273 SLC2A12
    nsv5395800mobile element insertion1nstd206human GRCh38 chr6: 133,990,918-133,990,969 , GRCh37.p13 chr6: 134,312,056-134,312,107 TBPL1, SLC2A12
    nsv5369784translocation1nstd200human GRCh38 chr6: 134,032,421-134,032,421 , GRCh38 chr6: 134,032,471-134,032,471 , GRCh37.p13 chr6: 134,353,559-134,353,559 , GRCh37.p13 chr6: 134,353,609-134,353,609 SLC2A12
    nsv5331676translocation1nstd200human GRCh37 chr6: 134,353,559-134,353,559 , GRCh37 chr6: 134,353,609-134,353,609 , GRCh38.p12 chr6: 134,032,471-134,032,471 , GRCh38.p12 chr6: 134,032,421-134,032,421 SLC2A12
    nsv5328814translocation1nstd204human GRCh38.p13 chr6: 134,032,471-134,032,471 , GRCh38.p13 chr6: 134,032,421-134,032,421 , GRCh37.p13 chr6: 134,353,609-134,353,609 , GRCh37.p13 chr6: 134,353,559-134,353,559 SLC2A12
    nsv5112957mobile element insertion1nstd203human GRCh38 chr6: 133,986,489-133,986,505 , GRCh37.p13 chr6: 134,307,627-134,307,643 SLC2A12, TBPL1
    nsv5108895mobile element insertion1nstd203human GRCh38 chr6: 133,996,696-133,996,705 , GRCh37.p13 chr6: 134,317,834-134,317,843 SLC2A12
    nsv5101042mobile element insertion1nstd203human GRCh38 chr6: 133,990,904-133,990,918 , GRCh37.p13 chr6: 134,312,042-134,312,056 TBPL1, SLC2A12
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4826537copy number variation1nstd200human GRCh37 chr6: 134,351,959-134,354,266 , GRCh38.p12 chr6: 134,030,821-134,033,128 SLC2A12
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