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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147180insertion1nstd232human GRCh37.p13 chr3: 128,889,416-128,889,416 , GRCh38.p12 chr3: 129,170,573-129,170,573 CNBP
    nsv7145422insertion1nstd232human GRCh37.p13 chr3: 128,890,617-128,890,617 , GRCh38.p12 chr3: 129,171,774-129,171,774 CNBP
    nsv7138292copy number variation1nstd232human GRCh37.p13 chr3: 128,890,379-128,890,473 , GRCh38.p12 chr3: 129,171,536-129,171,630 CNBP
    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
    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
    nsv6732135copy number variation1nstd229human GRCh38 chr3: 129,171,891-129,171,926 , GRCh37.p13 chr3: 128,890,734-128,890,769 CNBP
    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
    nsv6723083copy number variation1nstd229human GRCh38 chr3: 129,173,269-129,173,640 , GRCh37.p13 chr3: 128,892,112-128,892,483 CNBP
    nsv6722175copy number variation1nstd229human GRCh38 chr3: 129,170,531-129,171,158 , GRCh37.p13 chr3: 128,889,374-128,890,001 CNBP
    nsv6720321copy number variation1nstd229human GRCh38 chr3: 129,171,540-129,171,637 , GRCh37.p13 chr3: 128,890,383-128,890,480 CNBP
    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
    nsv6559324inversion1nstd223human GRCh38 chr3: 129,175,052-129,175,579 , GRCh37.p13 chr3: 128,893,895-128,894,422 CNBP
    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
    nsv6134783copy number variation1nstd213human GRCh37 chr3: 128,240,000-130,600,001 , GRCh38.p12 chr3: 128,521,157-130,881,157 FTH1P4, GP9, 68 more genes
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