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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
    nsv6736187copy number variation1nstd229human GRCh38 chr3: 130,044,539-130,087,905 , GRCh37.p13 chr3: 129,763,382-129,806,748 ALG1L2, LINC02014
    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
    nsv6725820copy number variation1nstd229human GRCh38 chr3: 130,087,209-130,089,123 , GRCh37.p13 chr3: 129,806,052-129,807,966 ALG1L2, LINC02014
    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
    nsv6373997copy number variation1nstd223human GRCh38 chr3: 130,083,901-130,087,600 , GRCh37.p13 chr3: 129,802,744-129,806,443 LINC02014, ALG1L2
    nsv6372286copy number variation1nstd223human GRCh38 chr3: 130,077,101-130,089,000 , GRCh37.p13 chr3: 129,795,944-129,807,843 LINC02014, ALG1L2
    nsv6371662copy number variation1nstd223human GRCh38 chr3: 130,080,601-130,089,200 , GRCh37.p13 chr3: 129,799,444-129,808,043 LINC02014, ALG1L2
    nsv6364318copy number variation1nstd223human GRCh38 chr3: 130,044,537-130,087,902 , GRCh37.p13 chr3: 129,763,380-129,806,745 LINC02014, ALG1L2
    nsv6361148copy number variation1nstd223human GRCh38 chr3: 130,083,101-130,087,600 , GRCh37.p13 chr3: 129,801,944-129,806,443 LINC02014, ALG1L2
    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
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