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Items: 1 to 20 of 124

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965429insertion1nstd209human GRCh38 chr6: 28,531,173-28,531,173 , GRCh37.p13 chr6: 28,498,950-28,498,950 GPX5
    nsv5730678mobile element insertion1nstd211human GRCh38 chr6: 28,529,744-28,529,744 , GRCh37.p13 chr6: 28,497,521-28,497,521 GPX5
    nsv5642595insertion1nstd207human GRCh38 chr6: 28,531,173-28,531,173 , GRCh37.p13 chr6: 28,498,950-28,498,950 GPX5
    nsv5557091mobile element insertion1nstd206human GRCh38 chr6: 28,529,754-28,529,795 , GRCh37.p13 chr6: 28,497,531-28,497,572 GPX5
    nsv5319891copy number variation1nstd204human GRCh38.p13 chr6: 28,528,797-28,530,945 , GRCh37.p13 chr6: 28,496,574-28,498,722 GPX5
    nsv5228736copy number variation1nstd204human GRCh38.p13 chr6: 28,528,937-28,531,071 , GRCh37.p13 chr6: 28,496,714-28,498,848 GPX5
    nsv5113166mobile element insertion1nstd203human GRCh38 chr6: 28,531,180-28,531,227 , GRCh37.p13 chr6: 28,498,957-28,499,004 GPX5
    nsv5106375mobile element insertion1nstd203human GRCh38 chr6: 28,531,165-28,531,173 , GRCh37.p13 chr6: 28,498,942-28,498,950 GPX5
    nsv5036471inversion1nstd200human GRCh38 chr6: 25,888,426-29,704,316 , GRCh37.p13 chr6: 25,888,654-29,672,093 , OR11A1, 368 more genes
    nsv4879678inversion1nstd200human GRCh37 chr6: 25,888,654-29,672,093 , GRCh38.p12 chr6: 25,888,426-29,704,316 , H1-4, 368 more genes
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4378463copy number variation1nstd173human GRCh37 chr6: 28,409,344-28,523,625 , GRCh38.p12 chr6: 28,441,567-28,555,848 OR2E1P, TRMEP1, 11 more genes
    nsv4366948copy number variation1nstd173human GRCh37 chr6: 28,418,991-28,523,625 , GRCh38.p12 chr6: 28,451,214-28,555,848 TRL-AAG4-1, TRT-CGT1-1, 9 more genes
    nsv3933730copy number variation1nstd167human GRCh37 chr6: 28,496,589-28,496,620 , GRCh38.p12 chr6: 28,528,812-28,528,843 GPX5
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 more genes
    nsv3915580copy number variation1nstd102humanUncertain significance NCBI36 chr6: 28,516,623-28,779,629 , GRCh37.p13 chr6: 28,408,644-28,671,650 , GRCh38.p12 chr6: 28,440,867-28,703,873 SCAND3, TRK-TTT13-1, 24 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
    nsv3911053copy number variation1nstd102humanUncertain significance GRCh38 chr6: 26,280,579-28,727,313 , GRCh37 chr6: 26,280,807-28,695,090 , NCBI36 chr6: 26,388,786-28,803,069 GPX5, TRI-AAT9-1, 232 more genes
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