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Items: 1 to 20 of 94

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7052094inversion1nstd229human GRCh38 chr3: 132,609,279-139,052,095 , GRCh37.p13 chr3: 132,328,123-138,770,937 RNU6-789P, UBA5, 98 more genes
    nsv7048686inversion1nstd229human GRCh38 chr3: 133,888,140-134,120,089 , GRCh37.p13 chr3: 133,606,984-133,838,933 LOC105374117, SLCO2A1, 3 more genes
    nsv7044513inversion1nstd229human GRCh38 chr3: 131,210,998-138,882,695 , GRCh37.p13 chr3: 130,929,842-138,601,537 HSPA8P9, RNU6-1174P, 114 more genes
    nsv7041788inversion1nstd229human GRCh38 chr3: 133,903,647-134,206,077 , GRCh37.p13 chr3: 133,622,491-133,924,921 C3orf36, LINC02000, 4 more genes
    nsv7039302inversion1nstd229human GRCh38 chr3: 133,378,933-139,551,784 , GRCh37.p13 chr3: 133,097,777-139,270,626 ESYT3, DONSONP1, 99 more genes
    nsv6724830copy number variation1nstd229human GRCh38 chr3: 133,865,649-133,944,841 , GRCh37.p13 chr3: 133,584,493-133,663,685 RAB6B, SLCO2A1, 1 more genes
    nsv6722777copy number variation1nstd229human GRCh38 chr3: 133,888,101-133,945,500 , GRCh37.p13 chr3: 133,606,945-133,664,344 C3orf36, RAB6B, 1 more genes
    nsv6720485copy number variation1nstd229human GRCh38 chr3: 133,924,401-134,005,800 , GRCh37.p13 chr3: 133,643,245-133,724,644 SLCO2A1, C3orf36
    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
    nsv6134784copy number variation1nstd213human GRCh37 chr3: 133,070,000-134,020,001 , GRCh38.p12 chr3: 133,351,156-134,301,159 RYK, SLCO2A1, 19 more genes
    nsv6134403copy number variation1nstd213human GRCh37 chr3: 133,600,000-135,410,001 , GRCh38.p12 chr3: 133,881,156-135,691,159 RAB6B, KY, 23 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
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4565249sequence alteration1nstd166human GRCh37.p13 chr3: 133,645,469-133,647,113 , GRCh38.p12 chr3: 133,926,625-133,928,269 C3orf36
    nsv4450267copy number variation1nstd102humanUncertain significance GRCh37 chr3: 133,588,698-133,662,948 , GRCh38.p12 chr3: 133,869,854-133,944,104 C3orf36, RAB6B, 1 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4327115inversion1nstd166human GRCh37.p13 chr3: 131,882,701-162,233,318 , GRCh38.p12 chr3: 132,163,857-162,515,530 , ATP1B3, 446 more genes
    nsv4095423copy number variation1nstd166human GRCh37.p13 chr3: 133,584,493-133,663,687 , GRCh38.p12 chr3: 133,865,649-133,944,843 SLCO2A1, RAB6B, 1 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
    nsv3921297copy number variation1nstd102humanPathogenic NCBI36 chr3: 133,918,512-145,986,275 , GRCh38 chr3: 132,716,978-144,784,743 , GRCh37 chr3: 132,435,822-144,503,585 BFSP2, YWHAQP6, 169 more genes
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