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Items: 1 to 20 of 222

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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
    nsv7096692copy number variation1nstd102humanPathogenic GRCh37 chr3: 128,603,476-128,603,609 , GRCh38.p12 chr3: 128,884,633-128,884,766 ACAD9
    nsv7096534copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 128,615,269-128,629,666 , GRCh38.p12 chr3: 128,896,426-128,910,823 ACAD9, CFAP92
    nsv7093533insertion1nstd102humanPathogenic GRCh37 chr3: 128,631,378-128,631,378 , GRCh38 chr3: 128,912,535-128,912,535 ACAD9, CFAP92
    nsv7093431delins1nstd102humanLikely pathogenic GRCh37 chr3: 128,628,971-128,629,505 , GRCh38 chr3: 128,910,128-128,910,662 ACAD9, CFAP92
    nsv7054855inversion1nstd229human GRCh38 chr3: 126,549,793-129,163,254 , GRCh37.p13 chr3: 126,268,636-128,882,097 RNA5SP139, LOC102723759, 63 more genes
    nsv7044884inversion1nstd229human GRCh38 chr3: 128,831,569-128,963,090 , GRCh37.p13 chr3: 128,550,412-128,681,933 MARK2P17, MIR12124, 5 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
    nsv7041415inversion1nstd229human GRCh38 chr3: 128,855,871-129,481,105 , GRCh37.p13 chr3: 128,574,714-129,199,948 CFAP92, H1-10, 24 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
    nsv6738042copy number variation1nstd229human GRCh38 chr3: 128,885,797-128,890,405 , GRCh37.p13 chr3: 128,604,640-128,609,248 ACAD9
    nsv6736891copy number variation1nstd229human GRCh38 chr3: 128,810,701-129,163,300 , GRCh37.p13 chr3: 128,529,544-128,882,143 EFCC1, ISY1, 12 more genes
    nsv6729391copy number variation1nstd229human GRCh38 chr3: 128,756,001-129,176,200 , GRCh37.p13 chr3: 128,474,844-128,895,043 CNBP, RN7SL698P, 16 more genes
    nsv6727194copy number variation1nstd229human GRCh38 chr3: 128,752,538-128,993,599 , GRCh37.p13 chr3: 128,471,381-128,712,442 MARK2P17, RN7SL698P, 9 more genes
    nsv6726764copy number variation1nstd229human GRCh38 chr3: 128,896,177-128,900,211 , GRCh37.p13 chr3: 128,615,020-128,619,054 ACAD9
    nsv6719441copy number variation1nstd229human GRCh38 chr3: 128,909,895-128,939,705 , GRCh37.p13 chr3: 128,628,738-128,658,548 ACAD9, CFAP92
    nsv6718180copy number variation1nstd229human GRCh38 chr3: 128,912,533-128,912,650 , GRCh37.p13 chr3: 128,631,376-128,631,493 ACAD9, CFAP92
    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
    nsv6637113copy number variation1nstd102humanUncertain significance GRCh37 chr3: 128,471,824-128,710,382 , GRCh38.p12 chr3: 128,752,981-128,991,539 RAB7A, MARK3P3, 9 more genes
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