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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3919629copy number variation1nstd102humanBenign GRCh38 chr8: 9,095,400-9,124,781 , GRCh37 chr8: 8,952,910-8,982,291 , NCBI36 chr8: 8,990,320-9,019,701 ERI1
    nsv3900803copy number variation1nstd102humanBenign GRCh37 chr8: 8,747,894-8,751,316 , GRCh38.p12 chr8|NW_018654717.1: 4,458,165-4,461,587 , GRCh38.p12 chr8: 8,890,384-8,893,806 ERI1, MFHAS1
    nsv3905092copy number variation1nstd102humanBenign GRCh37 chr8: 8,747,894-8,750,788 , GRCh38.p12 chr8: 8,890,384-8,893,278 , GRCh38.p12 chr8|NW_018654717.1: 4,458,693-4,461,587 ERI1, MFHAS1
    nsv3894030copy number variation1nstd102humanBenign GRCh37 chr8: 8,747,894-8,750,467 , GRCh38.p12 chr8: 8,890,384-8,892,957 , GRCh38.p12 chr8|NW_018654717.1: 4,459,014-4,461,587 ERI1, MFHAS1
    nsv3903224copy number variation1nstd102humanBenign GRCh37 chr8: 8,747,894-8,750,343 , GRCh38.p12 chr8|NW_018654717.1: 4,459,138-4,461,587 , GRCh38.p12 chr8: 8,890,384-8,892,833 ERI1, MFHAS1
    nsv3890767copy number variation1nstd102humanBenign GRCh37 chr8: 8,749,969-8,750,788 , GRCh38.p12 chr8|NW_018654717.1: 4,458,693-4,459,512 , GRCh38.p12 chr8: 8,892,459-8,893,278 ERI1, MFHAS1
    nsv3904720copy number variation1nstd102humanBenign GRCh37 chr8: 8,749,969-8,750,467 , GRCh38.p12 chr8|NW_018654717.1: 4,459,014-4,459,512 , GRCh38.p12 chr8: 8,892,459-8,892,957 ERI1, MFHAS1
    nsv3904744copy number variation1nstd102humanBenign GRCh37 chr8: 8,749,969-8,750,343 , GRCh38.p12 chr8|NW_018654717.1: 4,459,138-4,459,512 , GRCh38.p12 chr8: 8,892,459-8,892,833 ERI1, MFHAS1
    nsv3885208copy number variation1nstd102humanLikely benign GRCh37 chr8: 8,790,358-8,891,761 , GRCh38 chr8: 8,932,848-9,034,251 ERI1, RPL10P19, 2 more genes
    nsv4675381copy number variation1nstd102humanLikely benign GRCh37 chr8: 8,812,264-8,867,363 , GRCh38.p12 chr8: 8,954,754-9,009,853 , GRCh38.p12 chr8|NW_018654717.1: 4,342,106-4,397,198 ERI1, RPL10P19, 1 more genes
    nsv3915617copy number variation1nstd102humanLikely benign NCBI36 chr8: 8,774,342-8,797,685 , GRCh37 chr8: 8,736,932-8,760,275 , GRCh38 chr8: 8,879,422-8,902,765 ERI1, RNU6-682P, 1 more genes
    nsv3905193copy number variation1nstd102humanBenign GRCh37 chr8: 8,747,894-8,752,684 , GRCh38.p12 chr8: 8,890,384-8,895,174 , GRCh38.p12 chr8|NW_018654717.1: 4,456,797-4,461,587 ERI1, MFHAS1, 1 more genes
    nsv3900858copy number variation1nstd102humanBenign GRCh37 chr8: 8,747,894-8,752,587 , GRCh38.p12 chr8: 8,890,384-8,895,077 , GRCh38.p12 chr8|NW_018654717.1: 4,456,894-4,461,587 ERI1, RNU6-682P, 1 more genes
    nsv3908458copy number variation1nstd102humanBenign GRCh37 chr8: 8,749,969-8,752,587 , GRCh38.p12 chr8: 8,892,459-8,895,077 , GRCh38.p12 chr8|NW_018654717.1: 4,456,894-4,459,512 ERI1, RNU6-682P, 1 more genes
    nsv4455552copy number variation1nstd102humanUncertain significance GRCh37 chr8: 8,689,620-8,779,328 , GRCh38.p12 chr8: 8,832,110-8,921,818 , GRCh38.p12 chr8|NW_018654717.1: 4,430,134-4,519,890 ERI1, RNU6-682P, 1 more genes
    nsv6315449copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940 ERI1, LOC101928016, 568 more genes
    nsv3917350copy number variation2nstd102humanPathogenic GRCh37 chr8: 2,292,235-27,361,796 , GRCh38 chr8: 2,475,295-27,504,279 , NCBI36 chr8: 2,121,457-27,417,713 ERI1, LINC03022, 472 more genes
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 ERI1, ENTPD4, 447 more genes
    nsv6636968copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,049-18,936,715 , GRCh38.p12 chr8: 208,049-19,079,205 ERI1, ZNF705B, 357 more genes
    nsv4455719copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-14,214,722 , GRCh38.p12 chr8: 208,048-14,357,213 ERI1, MIR598, 312 more genes
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