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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965100insertion1nstd209human GRCh38 chr6: 149,275,139-149,275,139 , GRCh37.p13 chr6: 149,596,275-149,596,275 TAB2
    nsv5905197copy number variation1nstd209human GRCh38 chr6: 149,311,642-149,311,807 , GRCh37.p13 chr6: 149,632,778-149,632,943 TAB2
    nsv5902721copy number variation1nstd209human GRCh38 chr6: 149,366,702-149,367,410 , GRCh37.p13 chr6: 149,687,838-149,688,546 TAB2
    nsv5901089copy number variation1nstd209human GRCh38 chr6: 149,314,944-149,315,356 , GRCh37.p13 chr6: 149,636,080-149,636,492 TAB2
    nsv5888151copy number variation1nstd209human GRCh38 chr6: 149,226,079-149,226,397 , GRCh37.p13 chr6: 149,547,215-149,547,533 TAB2
    nsv5718602mobile element insertion1nstd211human GRCh38 chr6: 149,380,876-149,380,876 , GRCh37.p13 chr6: 149,702,012-149,702,012 TAB2
    nsv5681673mobile element insertion1nstd211human GRCh38 chr6: 149,228,555-149,228,555 , GRCh37.p13 chr6: 149,549,691-149,549,691 TAB2
    nsv5680055mobile element insertion1nstd211human GRCh38 chr6: 149,315,858-149,315,858 , GRCh37.p13 chr6: 149,636,994-149,636,994 TAB2
    nsv5582947copy number variation1nstd207human GRCh38 chr6: 149,311,642-149,311,807 , GRCh37.p13 chr6: 149,632,778-149,632,943 TAB2
    nsv5555585mobile element insertion1nstd206human GRCh38 chr6: 149,380,876-149,380,927 , GRCh37.p13 chr6: 149,702,012-149,702,063 TAB2
    nsv5473425copy number variation1nstd206human GRCh38 chr6: 149,355,632-149,364,578 , GRCh37.p13 chr6: 149,676,768-149,685,714 TAB2
    nsv5470986copy number variation1nstd206human GRCh38 chr6: 149,226,079-149,226,403 , GRCh37.p13 chr6: 149,547,215-149,547,539 TAB2
    nsv5469270copy number variation1nstd206human GRCh38 chr6: 149,311,646-149,311,808 , GRCh37.p13 chr6: 149,632,782-149,632,944 TAB2
    nsv5457073copy number variation1nstd206human GRCh38 chr6: 149,396,688-149,396,795 , GRCh37.p13 chr6: 149,717,824-149,717,931 TAB2
    nsv5409162mobile element insertion1nstd206human GRCh38 chr6: 149,228,555-149,228,606 , GRCh37.p13 chr6: 149,549,691-149,549,742 TAB2
    nsv5402282mobile element insertion1nstd206human GRCh38 chr6: 149,315,858-149,315,909 , GRCh37.p13 chr6: 149,636,994-149,637,045 TAB2
    nsv5369903translocation1nstd200human GRCh38 chr6: 149,323,918-149,323,918 , GRCh38 chr6: 149,323,765-149,323,765 , GRCh37.p13 chr6: 149,644,901-149,644,901 , GRCh37.p13 chr6: 149,645,054-149,645,054 TAB2
    nsv5330289translocation1nstd200human GRCh37 chr6: 149,645,054-149,645,054 , GRCh37 chr6: 149,644,901-149,644,901 , GRCh38.p12 chr6: 149,323,918-149,323,918 , GRCh38.p12 chr6: 149,323,765-149,323,765 TAB2
    nsv5313578copy number variation1nstd204human GRCh38.p13 chr6: 149,311,646-149,311,808 , GRCh37.p13 chr6: 149,632,782-149,632,944 TAB2
    nsv5310606copy number variation1nstd204human GRCh38.p13 chr6: 149,376,532-149,377,878 , GRCh37.p13 chr6: 149,697,668-149,699,014 TAB2
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