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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962186insertion1nstd209human GRCh38 chr6: 158,169,686-158,169,686 , GRCh37.p13 chr6: 158,590,718-158,590,718 GTF2H5
    nsv5905747copy number variation1nstd209human GRCh38 chr6: 158,187,728-158,191,642 , GRCh37.p13 chr6: 158,608,760-158,612,674 GTF2H5
    nsv5898255copy number variation1nstd209human GRCh38 chr6: 158,193,120-158,193,197 , GRCh37.p13 chr6: 158,614,152-158,614,229 GTF2H5
    nsv5681495mobile element insertion2nstd211human GRCh38 chr6: 158,199,217-158,199,217 , GRCh37.p13 chr6: 158,620,249-158,620,249 GTF2H5
    nsv5639465insertion1nstd207human GRCh38 chr6: 158,169,686-158,169,686 , GRCh37.p13 chr6: 158,590,718-158,590,718 GTF2H5
    nsv5636809insertion1nstd207human GRCh38 chr6: 158,169,360-158,169,360 , GRCh37.p13 chr6: 158,590,392-158,590,392 GTF2H5
    nsv5631808insertion1nstd207human GRCh38 chr6: 158,169,586-158,169,586 , GRCh37.p13 chr6: 158,590,618-158,590,618 GTF2H5
    nsv5625343insertion1nstd207human GRCh38 chr6: 158,169,397-158,169,397 , GRCh37.p13 chr6: 158,590,429-158,590,429 GTF2H5
    nsv5624668insertion2nstd207human GRCh38 chr6: 158,169,680-158,169,680 , GRCh37.p13 chr6: 158,590,712-158,590,712 GTF2H5
    nsv5408126mobile element insertion1nstd206human GRCh38 chr6: 158,199,217-158,199,268 , GRCh37.p13 chr6: 158,620,249-158,620,300 GTF2H5
    nsv5310078copy number variation1nstd204human GRCh38.p13 chr6: 157,839,496-158,613,672 , GRCh37.p13 chr6: 158,260,528-159,034,704 CACYBPP3, SYNJ2, 14 more genes
    nsv5238361copy number variation1nstd204human GRCh38.p13 chr6: 158,193,475-158,203,332 , GRCh37.p13 chr6: 158,614,507-158,624,364 GTF2H5
    nsv5108545mobile element insertion1nstd203human GRCh38 chr6: 158,193,204-158,193,210 , GRCh37.p13 chr6: 158,614,236-158,614,242 GTF2H5
    nsv5105053mobile element insertion1nstd203human GRCh38 chr6: 158,199,201-158,199,217 , GRCh37.p13 chr6: 158,620,233-158,620,249 GTF2H5
    nsv5100673mobile element insertion1nstd203human GRCh38 chr6: 158,181,182-158,181,195 , GRCh37.p13 chr6: 158,602,214-158,602,227 GTF2H5
    nsv4945880copy number variation1nstd200human GRCh38 chr6: 157,839,506-158,613,666 , GRCh37.p13 chr6: 158,260,538-159,034,698 CACYBPP3, SYNJ2-IT1, 14 more genes
    nsv4824831copy number variation1nstd200human GRCh37 chr6: 158,260,538-159,034,698 , GRCh38.p12 chr6: 157,839,506-158,613,666 SNX9, SYNJ2-IT1, 14 more genes
    nsv4766814inversion1nstd199human GRCh37 chr6: 153,752,140-161,206,728 , GRCh38.p12 chr6: 153,431,005-160,785,696 , ACAT2, 111 more genes
    nsv4675916copy number variation1nstd102humanUncertain significance GRCh37 chr6: 158,595,235-158,824,107 , GRCh38.p12 chr6: 158,174,203-158,403,075 SRP72P2, TULP4, 2 more genes
    nsv4602489copy number variation1nstd183human GRCh37 chr6: 158,589,378-158,589,531 , GRCh38.p12 chr6: 158,168,346-158,168,499 SERAC1, GTF2H5
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