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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096931copy number variation2nstd102humanUncertain significance GRCh37 chr3: 126,707,437-130,720,194 , GRCh38.p12 chr3: 126,988,594-131,001,350 JMJD4P1, MARK2P19, 104 more genes
    nsv7043614inversion1nstd229human GRCh38 chr3: 126,481,308-130,612,264 , GRCh37.p13 chr3: 126,200,151-130,331,108 SNRPCP8, CNBP, 106 more genes
    nsv6733069copy number variation1nstd229human GRCh38 chr3: 130,041,401-130,112,700 , GRCh37.p13 chr3: 129,760,244-129,831,543 LINC02014, ALG1L2, 2 more genes
    nsv6725477copy number variation1nstd229human GRCh38 chr3: 130,038,101-130,113,100 , GRCh37.p13 chr3: 129,756,944-129,831,943 ALG1L2, LINC02014, 2 more genes
    nsv6725361copy number variation1nstd229human GRCh38 chr3: 130,042,201-130,112,800 , GRCh37.p13 chr3: 129,761,044-129,831,643 ALG1L2, LINC02014, 2 more genes
    nsv6724541copy number variation1nstd229human GRCh38 chr3: 130,044,501-130,112,900 , GRCh37.p13 chr3: 129,763,344-129,831,743 LINC02021, FAM86HP, 2 more genes
    nsv6722992copy number variation1nstd229human GRCh38 chr3: 129,849,750-130,548,385 , GRCh37.p13 chr3: 129,568,593-130,267,229 COL6A4P2, OR7E129P, 17 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6566785inversion1nstd223human GRCh38 chr3: 125,931,297-130,096,571 , GRCh37.p13 chr3: 125,650,140-129,815,414 MIR6826, RN7SL698P, 114 more genes
    nsv6563554inversion1nstd223human GRCh38 chr3: 126,481,307-130,612,263 , GRCh37.p13 chr3: 126,200,150-130,331,107 METTL5P2, EFCC1, 106 more genes
    nsv6311770copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,365,818-133,465,047 , GRCh38.p12 chr3: 120,646,971-133,746,203 HNRNPA1P23, MIX23, 278 more genes
    nsv6160552copy number variation1nstd214human GRCh38 chr3: 130,098,813-130,098,864 , GRCh37.p13 chr3: 129,817,656-129,817,707 ALG1L2, FAM86HP
    nsv6160121copy number variation1nstd214human GRCh38 chr3: 130,098,761-130,098,864 , GRCh37.p13 chr3: 129,817,604-129,817,707 FAM86HP, ALG1L2
    nsv6155811copy number variation1nstd214human GRCh38 chr3: 130,098,737-130,098,788 , GRCh37.p13 chr3: 129,817,580-129,817,631 ALG1L2, FAM86HP
    nsv6134783copy number variation1nstd213human GRCh37 chr3: 128,240,000-130,600,001 , GRCh38.p12 chr3: 128,521,157-130,881,157 FTH1P4, GP9, 68 more genes
    nsv6134575copy number variation1nstd213human GRCh37 chr3: 116,870,000-132,100,001 , GRCh38.p12 chr3: 117,151,153-132,381,157 ACP3, ADCY5, 308 more genes
    nsv6112714copy number variation1nstd102humanPathogenic GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481 RNU6-789P, FAM86HP, 169 more genes
    nsv5991760copy number variation1nstd212human GRCh38 chr3: 130,104,109-130,104,187 , GRCh37.p13 chr3: 129,822,952-129,823,030 FAM86HP, ALG1L2
    nsv5991759copy number variation1nstd212human GRCh38 chr3: 130,098,789-130,098,842 , GRCh37.p13 chr3: 129,817,632-129,817,685 ALG1L2, FAM86HP
    nsv5583829copy number variation1nstd207human GRCh38 chr3: 130,104,114-130,104,190 , GRCh37.p13 chr3: 129,822,957-129,823,033 FAM86HP, ALG1L2
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