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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
    nsv7055739inversion1nstd229human GRCh38 chr3: 128,270,148-128,278,317 , GRCh37.p13 chr3: 127,988,991-127,997,160 EEFSEC
    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
    nsv7044958inversion1nstd229human GRCh38 chr3: 128,341,125-128,420,564 , GRCh37.p13 chr3: 128,059,968-128,139,407 EEFSEC
    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
    nsv6737819copy number variation1nstd229human GRCh38 chr3: 128,331,301-128,463,100 , GRCh37.p13 chr3: 128,050,144-128,181,943 DNAJB8, EEFSEC, 1 more genes
    nsv6737785copy number variation1nstd229human GRCh38 chr3: 128,341,101-128,461,000 , GRCh37.p13 chr3: 128,059,944-128,179,843 DNAJB8, EEFSEC
    nsv6736787copy number variation1nstd229human GRCh38 chr3: 127,816,252-128,456,391 , GRCh37.p13 chr3: 127,535,095-128,175,234 LOC102723759, RNA5SP139, 10 more genes
    nsv6734648copy number variation1nstd229human GRCh38 chr3: 128,412,331-128,419,015 , GRCh37.p13 chr3: 128,131,174-128,137,858 EEFSEC
    nsv6733729copy number variation1nstd229human GRCh38 chr3: 128,168,743-128,214,695 , GRCh37.p13 chr3: 127,887,586-127,933,538 EEFSEC
    nsv6731726copy number variation1nstd229human GRCh38 chr3: 128,406,749-128,409,240 , GRCh37.p13 chr3: 128,125,592-128,128,083 EEFSEC
    nsv6731073copy number variation1nstd229human GRCh38 chr3: 128,329,001-128,333,200 , GRCh37.p13 chr3: 128,047,844-128,052,043 EEFSEC
    nsv6728421copy number variation1nstd229human GRCh38 chr3: 128,351,837-128,372,714 , GRCh37.p13 chr3: 128,070,680-128,091,557 EEFSEC
    nsv6726690copy number variation1nstd229human GRCh38 chr3: 128,255,312-128,259,813 , GRCh37.p13 chr3: 127,974,155-127,978,656 EEFSEC
    nsv6724049copy number variation1nstd229human GRCh38 chr3: 128,379,991-128,385,616 , GRCh37.p13 chr3: 128,098,834-128,104,459 EEFSEC
    nsv6724047copy number variation1nstd229human GRCh38 chr3: 128,174,401-128,179,100 , GRCh37.p13 chr3: 127,893,244-127,897,943 EEFSEC
    nsv6723050copy number variation1nstd229human GRCh38 chr3: 128,307,366-128,308,116 , GRCh37.p13 chr3: 128,026,209-128,026,959 EEFSEC
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