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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1398107copy number variation1nstd102humanPathogenic GRCh37 (hg19) chr1: 45,794,977-45,798,996 , GRCh38 (hg38) chr1: 45,329,305-45,333,324 MUTYH
    nsv1197538complex substitution1nstd51humanPathogenic GRCh37 (hg19) chr1: 45,794,768-45,799,052 , GRCh38 (hg38) chr1: 45,329,096-45,333,380 MUTYH
    nsv1192077copy number variation1nstd113human NCBI36 (hg18) chr1: 45,506,183-45,728,432 , GRCh37 (hg19) chr1: 45,733,596-45,955,845 , GRCh38 (hg38) chr1: 45,267,924-45,490,173 TESK2, TOE1, 3 more genes
    nsv1188018copy number variation1nstd113human NCBI36 (hg18) chr1: 37,169,425-56,120,923 , GRCh37 (hg19) chr1: 37,396,838-56,348,335 , GRCh38 (hg38) chr1: 36,931,237-55,882,662 TRNAK-CUU, EFCAB14-AS1, 272 more genes
    nsv1146931inversion1nstd107human GRCh37 (hg19) chr1: 6,858,651-214,875,307 , GRCh38 (hg38) chr1: 6,798,591-214,701,964 MIR942, MIR190B, 2153 more genes
    nsv1133024inversion1nstd106human GRCh37 (hg19) chr1: 45,789,334-45,795,708 , GRCh38 (hg38) chr1: 45,323,662-45,330,036 MUTYH, HPDL
    nsv1132997inversion1nstd106human GRCh37 (hg19) chr1: 16,843,414-234,953,211 , GRCh38 (hg38) chr1: 16,516,919-234,817,464 MIR942, MIR190B, 2199 more genes
    nsv1130629copy number variation1nstd106human GRCh37 (hg19) chr1: 16,926,343-149,118,854 , GRCh38 (hg38) chr1: 16,599,848-149,532,129 MIR942, MIR760, 1149 more genes
    esv3671365novel sequence insertion1estd217human GRCh37 (hg19) chr1: 45,795,694-45,795,694 , GRCh38 (hg38) chr1: 45,330,022-45,330,022 MUTYH
    nsv1014509copy number variation1nstd100human NCBI36 (hg18) chr1: 45,460,110-45,660,088 , GRCh37 (hg19) chr1: 45,687,523-45,887,501 , GRCh38 (hg38) chr1: 45,221,851-45,421,829 TESK2, TOE1, 3 more genes
    nsv1012533copy number variation1nstd100human NCBI36 (hg18) chr1: 45,208,434-46,382,468 , GRCh37 (hg19) chr1: 45,435,847-46,609,881 , GRCh38 (hg38) chr1: 44,970,175-46,144,209 AKR1A1, TESK2, 18 more genes
    nsv1002433copy number variation1nstd100human NCBI36 (hg18) chr1: 37,169,425-56,120,923 , GRCh37 (hg19) chr1: 37,396,838-56,348,335 , GRCh38 (hg38) chr1: 36,931,237-55,882,662 TRNAK-CUU, EFCAB14-AS1, 271 more genes
    nsv999267copy number variation1nstd100human NCBI36 (hg18) chr1: 36,266,091-74,453,231 , GRCh37 (hg19) chr1: 36,493,504-74,680,643 , GRCh38 (hg38) chr1: 36,027,903-74,214,959 TRNAK-CUU, EFCAB14-AS1, 378 more genes
    nsv997548copy number variation1nstd100human NCBI36 (hg18) chr1: 45,506,183-45,728,432 , GRCh38 (hg38) chr1: 45,267,924-45,490,173 , GRCh37 (hg19) chr1: 45,733,596-45,955,845 TESK2, TOE1, 3 more genes
    nsv985916mobile element insertion37nstd94human GRCh37 (hg19) chr1: 45,795,708-45,795,709 , GRCh38 (hg38) chr1: 45,330,036-45,330,037 MUTYH
    nsv984836copy number variation2nstd11humannot provided NCBI36 (hg18) chr1: 51,598-247,191,011 , GRCh37 (hg19) chr1: 61,735-249,224,388 , GRCh38 (hg38) chr1: 61,735-248,930,189 AKT3, MIR942, 2594 more genes
    nsv984625complex substitution1nstd92human GRCh37 (hg19) chr1: 82,154-51,782,000 , GRCh38 (hg38) chr1: 82,154-51,316,328 TRNAN-GUU, TRNAE-UUC, 823 more genes
    esv3413571copy number variation1estd59human NCBI36 (hg18) chr1: 17,103,968-143,245,698 , GRCh37 (hg19) chr1: 17,231,381-144,534,341 , GRCh38 (hg38) chr1: 16,904,886-206,307,236 MIR942, MIR190B, 1922 more genes
    esv2992511copy number variation1estd209human GRCh37 (hg19) chr1: 45,804,426-45,804,427 , GRCh38 (hg38) chr1: 45,338,754-45,338,755 MUTYH
    esv3249763insertion1estd209human GRCh37 (hg19) chr1: 45,804,240-45,804,240 , GRCh38 (hg38) chr1: 45,338,568-45,338,568 MUTYH
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