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Items: 1 to 20 of 105

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6112688copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144 RNU4-62P, MTCO1P29, 169 more genes
    nsv6112686copy number variation1nstd102humanPathogenic GRCh37 chr3: 127,889,037-128,565,901 , GRCh38.p12 chr3: 128,170,194-128,847,058 EEFSEC, MARK2P8, 16 more genes
    nsv5897082copy number variation1nstd209human GRCh38 chr3: 128,574,628-128,574,959 , GRCh37.p13 chr3: 128,293,471-128,293,802 LINC01565
    nsv5435642copy number variation1nstd206human GRCh38 chr3: 128,574,628-128,574,993 , GRCh37.p13 chr3: 128,293,471-128,293,836 LINC01565
    nsv5316764copy number variation1nstd204human GRCh38.p13 chr3: 128,515,182-128,985,140 , GRCh37.p13 chr3: 128,234,025-128,703,983 CFAP92, FTH1P4, 14 more genes
    nsv5239829copy number variation1nstd204human GRCh38.p13 chr3: 128,557,869-128,599,987 , GRCh37.p13 chr3: 128,276,712-128,318,830 LINC01565
    nsv5231169copy number variation1nstd204human GRCh38.p13 chr3: 128,514,801-128,660,200 , GRCh37.p13 chr3: 128,233,644-128,379,043 RPN1, LINC01565, 1 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4914736copy number variation1nstd200human GRCh38 chr3: 128,515,192-128,985,136 , GRCh37.p13 chr3: 128,234,035-128,703,979 POU5F1P6, ACAD9, 14 more genes
    nsv4794338copy number variation1nstd200human GRCh37 chr3: 128,234,035-128,703,979 , GRCh38.p12 chr3: 128,515,192-128,985,136 RAB7A, MARK3P3, 14 more genes
    nsv4790976copy number variation1nstd200human GRCh37 chr3: 128,293,504-128,294,107 , GRCh38.p12 chr3: 128,574,661-128,575,264 LINC01565
    nsv4682915copy number variation1nstd102humanPathogenic GRCh37 chr3: 128,199,842-128,631,470 , GRCh38.p12 chr3: 128,480,999-128,912,627 MARK2P6, GATA2-AS1, 17 more genes
    nsv4521696copy number variation1nstd166human GRCh37.p13 chr3: 128,293,471-128,293,836 , GRCh38.p12 chr3: 128,574,628-128,574,993 LINC01565
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4326687inversion1nstd166human GRCh37.p13 chr3: 127,535,894-128,720,376 , GRCh38.p12 chr3: 127,817,051-129,001,533 RAB7A, MGLL, 32 more genes
    nsv4094658copy number variation1nstd166human GRCh37.p13 chr3: 128,291,000-128,322,500 , GRCh38.p12 chr3: 128,572,157-128,603,657 LINC01565
    nsv3923961copy number variation1nstd102humanPathogenic GRCh38 chr3: 126,797,420-128,946,623 , GRCh37 chr3: 126,516,263-128,665,466 , NCBI36 chr3: 127,998,953-130,148,156 RUVBL1-AS1, LOC105374096, 49 more genes
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
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