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Items: 1 to 20 of 1782

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3067543insertion1nstd90human GRCh37 (hg19) chr4: 69,959,841-69,959,841 , GRCh38 (hg38) chr4: 69,094,123-69,094,123 UGT2B7
    nsv3065774insertion1nstd140human GRCh37 (hg19) chr10: 101,587,734-101,587,735 , GRCh38 (hg38) chr10: 99,827,977-99,827,978 ABCC2
    nsv3064303insertion1nstd140human GRCh38 (hg38) chr10: 99,827,990-99,827,991 , GRCh37 (hg19) chr10: 101,587,747-101,587,748 ABCC2
    nsv3060084copy number variation1nstd140human GRCh37 (hg19) chr4: 69,959,843-69,960,167 , GRCh38 (hg38) chr4: 69,094,125-69,094,449 UGT2B7
    nsv3051291copy number variation1nstd140human GRCh38 (hg38) chr4: 69,094,127-69,094,451 , GRCh37 (hg19) chr4: 69,959,845-69,960,169 UGT2B7
    nsv3046450insertion1nstd140human GRCh38 (hg38) chr7: 87,626,709-87,626,710 , GRCh37 (hg19) chr7: 87,256,025-87,256,026 ABCB1
    nsv2817465insertion1nstd137human GRCh38 (hg38) chr7: 87,626,738-87,626,738 , GRCh37 (hg19) chr7: 87,256,054-87,256,054 ABCB1
    nsv2811219copy number variation1nstd137human GRCh38 (hg38) chr4: 69,094,125-69,094,448 , GRCh37 (hg19) chr4: 69,959,843-69,960,166 UGT2B7
    nsv2789693insertion1nstd137human GRCh38 (hg38) chr10: 99,839,153-99,839,153 , GRCh37 (hg19) chr10: 101,598,910-101,598,910 ABCC2
    nsv2789692insertion1nstd137human GRCh38 (hg38) chr10: 99,838,953-99,838,953 , GRCh37 (hg19) chr10: 101,598,710-101,598,710 ABCC2
    nsv2789691insertion1nstd137human GRCh38 (hg38) chr10: 99,814,541-99,814,541 , GRCh37 (hg19) chr10: 101,574,298-101,574,298 ABCC2
    nsv2789461insertion1nstd137human GRCh38 (hg38) chr10: 99,839,188-99,839,188 , GRCh37 (hg19) chr10: 101,598,945-101,598,945 ABCC2
    nsv2789460insertion1nstd137human GRCh38 (hg38) chr10: 99,838,929-99,838,929 , GRCh37 (hg19) chr10: 101,598,686-101,598,686 ABCC2
    nsv2789459insertion1nstd137human GRCh38 (hg38) chr10: 99,827,981-99,827,981 , GRCh37 (hg19) chr10: 101,587,738-101,587,738 ABCC2
    nsv2789458insertion1nstd137human GRCh38 (hg38) chr10: 99,814,656-99,814,656 , GRCh37 (hg19) chr10: 101,574,413-101,574,413 ABCC2
    nsv2789457copy number variation1nstd137human GRCh38 (hg38) chr10: 99,814,185-99,814,238 , GRCh37 (hg19) chr10: 101,573,942-101,573,995 ABCC2
    nsv2787932copy number variation1nstd132human NCBI36 (hg18) chr12: 21,221,005-21,222,816 , GRCh37 (hg19) chr12: 21,329,738-21,331,549 , GRCh38 (hg38) chr12: 21,176,804-21,178,615 SLCO1B1
    nsv2787666copy number variation1nstd132human NCBI36 (hg18) chr12: 21,186,879-21,200,724 , GRCh37 (hg19) chr12: 21,295,612-21,309,457 , GRCh38 (hg38) chr12: 21,142,678-21,156,523 SLCO1B1
    nsv2787356copy number variation1nstd132human NCBI36 (hg18) chr12: 21,088,684-21,206,711 , GRCh37 (hg19) chr12: 21,197,417-21,315,444 , GRCh38 (hg38) chr12: 21,044,483-21,162,510 SLCO1B1, SLCO1B7
    nsv2787147copy number variation1nstd132human NCBI36 (hg18) chr12: 21,185,560-21,208,619 , GRCh37 (hg19) chr12: 21,294,293-21,317,352 , GRCh38 (hg38) chr12: 21,141,359-21,164,418 SLCO1B1
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