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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5444598copy number variation1nstd206human GRCh38 chr3: 121,622,188-121,654,524 , GRCh37.p13 chr3: 121,341,035-121,373,371 RN7SL172P, HCLS1, 2 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5031637inversion1nstd200human GRCh38 chr3: 112,181,184-125,673,487 , GRCh37.p13 chr3: 111,900,031-125,392,331 , ARHGAP31, 218 more genes
    nsv4596004copy number variation1nstd183human GRCh37 chr3: 121,289,421-121,388,385 , GRCh38.p12 chr3: 121,570,574-121,669,538 GOLGB1, HCLS1, 4 more genes
    nsv4587190copy number variation1nstd183human GRCh37 chr3: 121,289,499-121,390,283 , GRCh38.p12 chr3: 121,570,652-121,671,436 GOLGB1, HCLS1, 4 more genes
    nsv4584691copy number variation1nstd183human GRCh37 chr3: 121,064,744-121,418,556 , GRCh38.p12 chr3: 121,345,897-121,699,709 ARGFX, ARPC1AP1, 8 more genes
    nsv4521011copy number variation1nstd166human GRCh37.p13 chr3: 121,284,999-121,394,000 , GRCh38.p12 chr3: 121,566,152-121,675,153 GOLGB1, HCLS1, 4 more genes
    nsv4410922copy number variation1nstd174human GRCh37 chr3: 121,289,499-121,390,271 , GRCh38.p12 chr3: 121,570,652-121,671,424 GOLGB1, HCLS1, 4 more genes
    nsv4396704copy number variation1nstd174human GRCh37 chr3: 121,070,299-121,434,434 , GRCh38.p12 chr3: 121,351,452-121,715,587 HCLS1, STXBP5L, 8 more genes
    nsv4382066copy number variation1nstd173human GRCh37 chr3: 121,338,814-121,374,032 , GRCh38.p12 chr3: 121,619,967-121,655,185 HCLS1, FBXO40, 2 more genes
    nsv4367735copy number variation1nstd173human GRCh37 chr3: 121,339,020-121,374,032 , GRCh38.p12 chr3: 121,620,173-121,655,185 FBXO40, RNU4-62P, 2 more genes
    nsv4317801inversion1nstd166human GRCh37.p13 chr3: 106,160,269-123,476,086 , GRCh38.p12 chr3: 106,441,422-123,757,239 , ADPRH, 270 more genes
    nsv4312526inversion1nstd166human GRCh37.p13 chr3: 121,211,040-121,605,532 , GRCh38.p12 chr3: 121,492,193-121,886,685 RPL7AP11, HCLS1, 8 more genes
    nsv4087776copy number variation1nstd166human GRCh37.p13 chr3: 120,845,680-121,576,564 , GRCh38.p12 chr3: 121,126,833-121,857,717 RN7SL172P, POLQ, 10 more genes
    nsv3963319insertion1nstd168human GRCh38 chr3: 121,644,499-121,677,766 , GRCh37.p13 chr3: 121,363,346-121,396,613 GOLGB1, HCLS1, 2 more genes
    nsv3924082copy number variation1nstd102humanPathogenic NCBI36 chr3: 119,875,435-127,742,263 , GRCh38 chr3: 118,673,898-126,540,730 , GRCh37 chr3: 118,392,745-126,259,573 MYLK-AS2, RPL7AP11, 165 more genes
    nsv3923097copy number variation1nstd102humanPathogenic NCBI36 chr3: 120,318,703-127,122,267 , GRCh38 chr3: 119,117,166-125,920,734 , GRCh37 chr3: 118,836,013-125,639,577 POGLUT1, RN7SL397P, 141 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
    nsv3919464copy number variation1nstd102humanPathogenic GRCh38 chr3: 114,122,562-124,532,374 , GRCh37 chr3: 113,841,409-124,251,221 , NCBI36 chr3: 115,324,099-125,733,911 B4GALT4-AS1, LSAMP, 144 more genes
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