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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
    nsv7043614inversion1nstd229human GRCh38 chr3: 126,481,308-130,612,264 , GRCh37.p13 chr3: 126,200,151-130,331,108 SNRPCP8, CNBP, 106 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
    nsv6737080copy number variation1nstd229human GRCh38 chr3: 129,598,818-129,599,279 , GRCh37.p13 chr3: 129,317,661-129,318,122 PLXND1
    nsv6732701copy number variation1nstd229human GRCh38 chr3: 129,596,836-129,596,907 , GRCh37.p13 chr3: 129,315,679-129,315,750 PLXND1
    nsv6722122copy number variation1nstd229human GRCh38 chr3: 129,549,099-129,566,407 , GRCh37.p13 chr3: 129,267,942-129,285,250 PLXND1, H1-8
    nsv6718713copy number variation1nstd229human GRCh38 chr3: 129,562,273-129,570,384 , GRCh37.p13 chr3: 129,281,116-129,289,227 PLXND1
    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
    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
    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
    nsv6134399copy number variation1nstd213human GRCh37 chr3: 128,260,000-129,620,001 , GRCh38.p12 chr3: 128,541,157-129,901,158 FTH1P4, GP9, 43 more genes
    nsv6112714copy number variation1nstd102humanPathogenic GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481 RNU6-789P, FAM86HP, 169 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
    nsv5991499copy number variation1nstd212human GRCh38 chr3: 129,574,890-129,575,342 , GRCh37.p13 chr3: 129,293,733-129,294,185 PLXND1
    nsv5899369copy number variation1nstd209human GRCh38 chr3: 129,596,836-129,596,906 , GRCh37.p13 chr3: 129,315,679-129,315,749 PLXND1
    nsv5442847copy number variation1nstd206human GRCh38 chr3: 129,596,844-129,596,907 , GRCh37.p13 chr3: 129,315,687-129,315,750 PLXND1
    nsv5090739mobile element insertion1nstd203human GRCh38 chr3: 129,594,389-129,594,403 , GRCh37.p13 chr3: 129,313,232-129,313,246 PLXND1
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