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Items: 1 to 20 of 213

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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
    nsv7044513inversion1nstd229human GRCh38 chr3: 131,210,998-138,882,695 , GRCh37.p13 chr3: 130,929,842-138,601,537 HSPA8P9, RNU6-1174P, 114 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
    nsv6737359copy number variation1nstd229human GRCh38 chr3: 133,796,828-133,797,583 , GRCh37.p13 chr3: 133,515,672-133,516,427 SRPRB, LOC105374116, 1 more genes
    nsv6731409copy number variation1nstd229human GRCh38 chr3: 133,801,965-133,801,996 , GRCh37.p13 chr3: 133,520,809-133,520,840 LOC105374116, SRPRB
    nsv6724951copy number variation1nstd229human GRCh38 chr3: 133,784,647-133,813,293 , GRCh37.p13 chr3: 133,503,491-133,532,137 SRPRB, LOC105374116, 1 more genes
    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
    nsv6364435copy number variation1nstd223human GRCh38 chr3: 133,808,293-133,808,869 , GRCh37.p13 chr3: 133,527,137-133,527,713 SRPRB
    nsv6254697mobile element insertion1nstd215human GRCh38 chr3: 133,815,208-133,815,208 , GRCh37.p13 chr3: 133,534,052-133,534,052 SRPRB
    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
    nsv6134494copy number variation1nstd213human GRCh37 chr3: 133,330,000-133,510,001 , GRCh38.p12 chr3: 133,611,156-133,791,157 TF, TOPBP1, 6 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
    nsv6063854insertion1nstd212human GRCh38 chr3: 133,785,312-133,785,312 , GRCh37.p13 chr3: 133,504,156-133,504,156 TF, SRPRB, 1 more genes
    nsv6060808insertion1nstd212human GRCh38 chr3: 133,785,405-133,785,405 , GRCh37.p13 chr3: 133,504,249-133,504,249 TF, SRPRB, 1 more genes
    nsv5991519copy number variation1nstd212human GRCh38 chr3: 133,785,338-133,785,412 , GRCh37.p13 chr3: 133,504,182-133,504,256 TF, SRPRB, 1 more genes
    nsv5991518copy number variation1nstd212human GRCh38 chr3: 133,784,932-133,786,247 , GRCh37.p13 chr3: 133,503,776-133,505,091 TF, SRPRB, 1 more genes
    nsv5991379copy number variation1nstd212human GRCh38 chr3: 133,808,655-133,808,785 , GRCh37.p13 chr3: 133,527,499-133,527,629 SRPRB
    nsv5991315copy number variation1nstd212human GRCh38 chr3: 133,785,399-133,785,454 , GRCh37.p13 chr3: 133,504,243-133,504,298 TF, SRPRB, 1 more genes
    nsv5896614copy number variation1nstd209human GRCh38 chr3: 133,808,293-133,808,868 , GRCh37.p13 chr3: 133,527,137-133,527,712 SRPRB
    nsv5718450mobile element insertion2nstd211human GRCh38 chr3: 133,784,473-133,784,473 , GRCh37.p13 chr3: 133,503,317-133,503,317 TF, SRPRB, 1 more genes
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