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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127749insertion1nstd186human GRCh37 chr5: 179,122,509-179,122,528 , GRCh38.p12 chr5|NW_016107298.1: 461,065-461,084 , GRCh38.p12 chr5: 179,695,508-179,695,527 CANX
    nsv5960587insertion1nstd209human GRCh38 chr5: 179,695,492-179,695,492 , GRCh37.p13 chr5: 179,122,493-179,122,493 CANX
    nsv5958460insertion1nstd209human GRCh38 chr5: 179,710,707-179,710,707 , GRCh37.p13 chr5: 179,137,708-179,137,708 CANX
    nsv5905046copy number variation1nstd209human GRCh38 chr5: 179,695,085-179,695,368 , GRCh37.p13 chr5: 179,122,086-179,122,369 HMGB3P22, CANX
    nsv5900453copy number variation1nstd209human GRCh38 chr5: 179,695,343-179,695,477 , GRCh37.p13 chr5: 179,122,344-179,122,478 CANX
    nsv5892629copy number variation1nstd209human GRCh38 chr5: 179,677,331-179,677,811 , GRCh37.p13 chr5: 179,104,332-179,104,812 CANX, CBY3
    nsv5891784copy number variation1nstd209human GRCh38 chr5: 179,683,309-179,683,707 , GRCh37.p13 chr5: 179,110,310-179,110,708 CANX
    nsv5889549copy number variation1nstd209human GRCh38 chr5: 179,693,332-179,693,465 , GRCh37.p13 chr5: 179,120,333-179,120,466 HMGB3P22, CANX
    nsv5722702mobile element insertion1nstd211human GRCh38 chr5: 179,715,067-179,715,067 , GRCh37.p13 chr5: 179,142,068-179,142,068 CANX
    nsv5566406copy number variation1nstd207human GRCh38 chr5: 179,693,332-179,693,465 , GRCh37.p13 chr5: 179,120,333-179,120,466 CANX, HMGB3P22
    nsv5561640sequence alteration1nstd206human GRCh38 chr5: 179,554,688-180,310,132 , GRCh37.p13 chr5: 178,981,689-179,737,132 HNRNPH1, MRNIP, 28 more genes
    nsv5554408mobile element insertion1nstd206human GRCh38 chr5: 179,715,067-179,715,118 , GRCh37.p13 chr5: 179,142,068-179,142,119 CANX
    nsv5536545insertion1nstd206human GRCh38 chr5: 179,695,508-179,695,527 , GRCh37.p13 chr5: 179,122,509-179,122,528 CANX
    nsv5470777copy number variation1nstd206human GRCh38 chr5: 179,680,424-179,680,474 , GRCh37.p13 chr5: 179,107,425-179,107,475 CANX, CBY3
    nsv5462349copy number variation1nstd206human GRCh38 chr5: 179,693,350-179,693,466 , GRCh37.p13 chr5: 179,120,351-179,120,467 CANX, HMGB3P22
    nsv5461442copy number variation1nstd206human GRCh38 chr5: 179,683,309-179,683,539 , GRCh37.p13 chr5: 179,110,310-179,110,540 CANX
    nsv5460387copy number variation1nstd206human GRCh38 chr5: 179,677,513-179,677,927 , GRCh37.p13 chr5: 179,104,514-179,104,928 CANX, CBY3
    nsv5381440copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,699,902-179,263,603 , GRCh38.p12 chr5: 179,272,901-179,836,603 , GRCh38.p12 chr5|NW_016107298.1: 37,608-602,163 LOC105377761, MGAT4B, 22 more genes
    nsv5381377copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,770,758-179,263,603 , GRCh38.p12 chr5: 179,343,757-179,836,603 , GRCh38.p12 chr5|NW_016107298.1: 108,464-602,163 LOC100289470, LOC100502572, 22 more genes
    nsv5312287copy number variation1nstd204human GRCh38.p13 chr5: 179,726,045-179,726,314 , GRCh37.p13 chr5: 179,153,046-179,153,315 CANX
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