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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054967inversion1nstd229human GRCh38 chr3: 126,359,907-128,810,656 , GRCh37.p13 chr3: 126,078,750-128,529,499 LOC107986129, RNU6-823P, 56 more genes
    nsv7054930inversion1nstd229human GRCh38 chr3: 126,390,504-126,393,114 , GRCh37.p13 chr3: 126,109,347-126,111,957 CFAP100, CFAP100-DT, 1 more genes
    nsv7050176inversion1nstd229human GRCh38 chr3: 126,388,052-126,391,219 , GRCh37.p13 chr3: 126,106,895-126,110,062 LOC107986044, CFAP100-DT
    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
    nsv6714190copy number variation1nstd229human GRCh38 chr3: 126,393,032-126,393,445 , GRCh37.p13 chr3: 126,111,875-126,112,288 CFAP100, CFAP100-DT
    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
    nsv6702525copy number variation1nstd229human GRCh38 chr3: 125,697,301-126,581,200 , GRCh37.p13 chr3: 125,416,145-126,300,043 CFAP100-DT, RNU1-30P, 36 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
    nsv6556022inversion1nstd223human GRCh38 chr3: 123,151,729-129,172,574 , GRCh37.p13 chr3: 122,870,576-128,891,417 UMPS, CHST13, 139 more genes
    nsv6313832copy number variation1nstd102humanUncertain significance GRCh37 chr3: 124,990,058-126,401,548 , GRCh38.p12 chr3: 125,271,214-126,682,705 LOC100419966, NUP210P1, 50 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
    nsv6134781copy number variation1nstd213human GRCh37 chr3: 125,950,000-127,090,001 , GRCh38.p12 chr3: 126,231,157-127,371,158 PLXNA1, KLF15, 22 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
    nsv6134490copy number variation1nstd213human GRCh37 chr3: 125,780,000-127,270,001 , GRCh38.p12 chr3: 126,061,157-127,551,158 PLXNA1, ALDH1L1, 33 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
    nsv5991728copy number variation1nstd212human GRCh38 chr3: 126,388,760-126,400,489 , GRCh37.p13 chr3: 126,107,603-126,119,332 CFAP100, CFAP100-DT, 1 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
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