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Items: 1 to 20 of 112

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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
    nsv7054967inversion1nstd229human GRCh38 chr3: 126,359,907-128,810,656 , GRCh37.p13 chr3: 126,078,750-128,529,499 LOC107986129, RNU6-823P, 56 more genes
    nsv7054855inversion1nstd229human GRCh38 chr3: 126,549,793-129,163,254 , GRCh37.p13 chr3: 126,268,636-128,882,097 RNA5SP139, LOC102723759, 63 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
    nsv7039961inversion1nstd229human GRCh38 chr3: 125,220,024-129,368,164 , GRCh37.p13 chr3: 124,938,868-129,087,007 MARK3P3, RAB43, 120 more genes
    nsv7038944inversion1nstd229human GRCh38 chr3: 125,715,935-130,031,043 , GRCh37.p13 chr3: 125,434,863-129,749,886 H1-8, FBRSL1P1, 123 more genes
    nsv6710779copy number variation1nstd229human GRCh38 chr3: 125,082,194-128,829,123 , GRCh37.p13 chr3: 124,801,038-128,547,966 LOC105374094, DNAJB8-AS1, 98 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
    nsv6556022inversion1nstd223human GRCh38 chr3: 123,151,729-129,172,574 , GRCh37.p13 chr3: 122,870,576-128,891,417 UMPS, CHST13, 139 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
    nsv6291058copy number variation1nstd102humanUncertain significance GRCh37 chr3: 128,163,252-128,660,960 , GRCh38.p12 chr3: 128,444,409-128,942,117 IFT122P3, DNAJB8, 19 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
    nsv6134398copy number variation1nstd213human GRCh37 chr3: 127,990,000-128,230,001 , GRCh38.p12 chr3: 128,271,157-128,511,158 , GRCh38.p12 chr3|NW_019805490.1: 140,261-302,885 GATA2, EEFSEC, 4 more genes
    nsv6134397copy number variation1nstd213human GRCh37 chr3: 127,950,000-128,340,001 , GRCh38.p12 chr3: 128,231,157-128,621,158 , GRCh38.p12 chr3|NW_019805490.1: 100,260-302,885 GATA2, RPN1, 7 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
    nsv6112709copy number variation1nstd102humanPathogenic GRCh37 chr3: 123,000,000-129,700,000 , GRCh38.p12 chr3: 123,281,153-129,981,157 OR7E97P, MARK3P3, 160 more genes
    nsv6112688copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144 RNU4-62P, MTCO1P29, 169 more genes
    nsv6112686copy number variation1nstd102humanPathogenic GRCh37 chr3: 127,889,037-128,565,901 , GRCh38.p12 chr3: 128,170,194-128,847,058 EEFSEC, MARK2P8, 16 more genes
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