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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143364insertion1nstd232human GRCh37.p13 chr6: 138,727,290-138,727,290 , GRCh38.p12 chr6: 138,406,153-138,406,153 HEBP2
    nsv7050559inversion1nstd229human GRCh38 chr6: 137,097,512-142,245,470 , GRCh37.p13 chr6: 137,418,649-142,566,607 LINC03004, LOC107986651, 64 more genes
    nsv6817262copy number variation1nstd229human GRCh38 chr6: 138,108,467-138,518,391 , GRCh37.p13 chr6: 138,429,604-138,839,528 MIR3145, PBOV1, 5 more genes
    nsv6815558copy number variation1nstd229human GRCh38 chr6: 138,312,875-138,532,860 , GRCh37.p13 chr6: 138,634,012-138,853,997 MARCKSL1P2, NHSL1, 4 more genes
    nsv6811912copy number variation1nstd229human GRCh38 chr6: 137,801,388-140,356,633 , GRCh37.p13 chr6: 138,122,525-140,677,770 TXLNB, LOC100129844, 38 more genes
    nsv6614953copy number variation1nstd223human GRCh38 chr6: 138,375,470-138,690,875 , GRCh37.p13 chr6: 138,696,607-139,012,012 HEBP2, NHSL1, 5 more genes
    nsv6314818copy number variation1nstd102humanPathogenic GRCh38 chr6: 134,838,331-142,160,056 , GRCh37.p13 chr6: 135,159,469-142,481,193 PBOV1, IFNGR1, 100 more genes
    nsv6313812copy number variation1nstd102humanUncertain significance GRCh37 chr6: 138,650,501-139,046,686 , GRCh38.p12 chr6: 138,329,364-138,725,549 NHSL1-AS1, MTCH1P1, 7 more genes
    nsv6135475copy number variation1nstd213human GRCh37 chr6: 138,530,000-139,120,001 , GRCh38.p12 chr6: 138,208,863-138,798,864 HEBP2, CCDC28A, 10 more genes
    nsv6112726copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,810,210-140,046,615 , GRCh38.p12 chr6: 133,489,072-139,725,478 SIMALR, MTFR2, 99 more genes
    nsv5893389copy number variation1nstd209human GRCh38 chr6: 137,986,656-139,086,959 , GRCh37.p13 chr6: 138,307,793-139,408,096 ECT2L, NHSL1-AS1, 17 more genes
    nsv5642353insertion1nstd207human GRCh38 chr6: 138,412,444-138,412,444 , GRCh37.p13 chr6: 138,733,581-138,733,581 HEBP2
    nsv5547815insertion1nstd206human GRCh38 chr6: 138,417,716-138,417,716 , GRCh37.p13 chr6: 138,738,853-138,738,853 HEBP2
    nsv5039909inversion1nstd200human GRCh38 chr6: 137,955,606-139,947,661 , GRCh37.p13 chr6: 138,276,743-140,268,798 , CCDC28A-AS1, 30 more genes
    nsv4945727copy number variation1nstd200human GRCh38 chr6: 138,321,715-138,427,804 , GRCh37.p13 chr6: 138,642,852-138,748,941 SMIM28, HEBP2, 3 more genes
    nsv4729511copy number variation1nstd102humanUncertain significance GRCh37 chr6: 138,396,174-138,736,943 , GRCh38.p12 chr6: 138,075,037-138,415,806 MARCKSL1P2, ARFGEF3, 4 more genes
    nsv4685709copy number variation1nstd102humannot provided GRCh37 chr6: 135,936,688-140,660,269 , GRCh38.p12 chr6: 135,615,550-140,339,132 MAP7, RN7SKP299, 74 more genes
    nsv4680132copy number variation1nstd189human GRCh37.p13 chr6: 138,484,930-139,143,192 , GRCh38.p12 chr6: 138,163,793-138,822,055 HEBP2, CCDC28A, 11 more genes
    nsv4678977copy number variation1nstd189human GRCh37.p13 chr6: 138,480,417-139,142,058 , GRCh38.p12 chr6: 138,159,280-138,820,921 HEBP2, CCDC28A, 11 more genes
    nsv4675250copy number variation1nstd102humanPathogenic GRCh37 chr6: 133,817,341-140,038,401 , GRCh38.p12 chr6: 133,496,203-139,717,264 ALDH8A1, IL22RA2, 99 more genes
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