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Items: 1 to 20 of 233

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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
    nsv7096440copy number variation1nstd102humanUncertain significance GRCh37 chr3: 126,707,437-127,783,900 , GRCh38.p12 chr3: 126,988,594-128,065,057 LOC105374094, RNU6-1047P, 23 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
    nsv7050658inversion1nstd229human GRCh38 chr3: 126,996,800-127,000,311 , GRCh37.p13 chr3: 126,715,643-126,719,154 PLXNA1
    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
    nsv6735481copy number variation1nstd229human GRCh38 chr3: 126,983,801-127,109,000 , GRCh37.p13 chr3: 126,702,644-126,827,843 PLXNA1
    nsv6733384copy number variation1nstd229human GRCh38 chr3: 126,951,544-127,017,511 , GRCh37.p13 chr3: 126,670,387-126,736,354 PLXNA1, CHCHD6
    nsv6728790copy number variation1nstd229human GRCh38 chr3: 126,997,301-126,999,700 , GRCh37.p13 chr3: 126,716,144-126,718,543 PLXNA1
    nsv6728038copy number variation1nstd229human GRCh38 chr3: 126,998,539-127,222,766 , GRCh37.p13 chr3: 126,717,382-126,941,609 PRR23E2P, PLXNA1, 1 more genes
    nsv6727629copy number variation1nstd229human GRCh38 chr3: 127,022,179-127,022,374 , GRCh37.p13 chr3: 126,741,022-126,741,217 PLXNA1
    nsv6727106copy number variation1nstd229human GRCh38 chr3: 126,990,247-126,991,053 , GRCh37.p13 chr3: 126,709,090-126,709,896 PLXNA1
    nsv6718835copy number variation1nstd229human GRCh38 chr3: 127,019,173-127,019,239 , GRCh37.p13 chr3: 126,738,016-126,738,082 PLXNA1
    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
    nsv6636901copy number variation1nstd102humanUncertain significance GRCh37 chr3: 126,269,767-126,800,773 , GRCh38.p12 chr3: 126,550,924-127,081,930 RCC2P4, RNA5SP138, 8 more genes
    nsv6635939copy number variation1nstd227human GRCh37 chr3: 126,695,646-126,732,047 , GRCh38.p12 chr3: 126,976,803-127,013,204 PLXNA1
    nsv6566785inversion1nstd223human GRCh38 chr3: 125,931,297-130,096,571 , GRCh37.p13 chr3: 125,650,140-129,815,414 MIR6826, RN7SL698P, 114 more genes
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