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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112759copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,001-8,472,742 , GRCh38.p12 chr3: 18,324-8,431,056 LOC105376926, LOC107986057, 69 more genes
    nsv5894841copy number variation1nstd209human GRCh38 chr3: 1,880,218-5,919,238 , GRCh37.p13 chr3: 1,921,902-5,960,925 , IL5RA, 37 more genes
    nsv5381423copy number variation1nstd102humanPathogenic GRCh37 chr3: 73,914-5,940,479 , GRCh38.p12 chr3: 32,241-5,898,792 ITPR1-DT, RPSAP32, 54 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4914240copy number variation1nstd200human GRCh38 chr3: 1,881,358-4,897,912 , GRCh37.p13 chr3: 1,923,042-4,939,596 , EGOT, 23 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4674799copy number variation1nstd102humanUncertain significance GRCh37 chr3: 4,240,739-4,707,310 , GRCh38.p12 chr3: 4,199,055-4,665,626 MRPS10P2, LOC105376933, 4 more genes
    nsv4674715copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-10,287,825 , GRCh38.p12 chr3: 20,213-10,246,141 LOC105376944, LMCD1, 122 more genes
    nsv4674167copy number variation1nstd102humanUncertain significance GRCh37 chr3: 3,511,130-4,915,785 , GRCh38.p12 chr3: 3,469,446-4,874,101 EGOT, ITPR1-DT, 9 more genes
    nsv4578467copy number variation1nstd102humanUncertain significance GRCh37 chr3: 4,213,134-4,571,031 , GRCh38.p12 chr3: 4,171,450-4,529,347 ITPR1, SETMAR, 3 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4519845copy number variation1nstd166human GRCh37.p13 chr3: 3,018,999-7,816,000 , GRCh38.p12 chr3: 2,977,315-7,774,313 , BHLHE40-AS1, 42 more genes
    nsv4453150copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,891-6,067,006 , GRCh38.p12 chr3: 20,213-6,025,319 LOC105376924, CRB3P1, 56 more genes
    nsv4452578copy number variation1nstd102humanUncertain significance GRCh37 chr3: 4,477,388-4,998,006 , GRCh38.p12 chr3: 4,435,704-4,956,321 ITPR1-DT, LOC105376933, 4 more genes
    nsv4451504copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,891-8,269,583 , GRCh38.p12 chr3: 20,213-8,227,896 LOC102723596, CHL1-AS1, 67 more genes
    nsv4450791copy number variation1nstd102humanPathogenic GRCh37 chr3: 4,513,497-4,612,609 , GRCh38.p12 chr3: 4,471,813-4,570,925 ITPR1, ITPR1-DT
    nsv4450477copy number variation1nstd102humanUncertain significance GRCh37 chr3: 4,294,669-4,785,230 , GRCh38.p12 chr3: 4,252,985-4,743,546 LOC105376933, MRPS10P2, 4 more genes
    nsv4449957copy number variation1nstd102humanPathogenic GRCh37 chr3: 4,276,014-4,643,555 , GRCh38.p12 chr3: 4,234,330-4,601,871 ITPR1, SETMAR, 4 more genes
    nsv4436544copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 36,016-9,307,855 , GRCh38.p12 chr3: 18,324-9,266,171 CAV3, GRM7, 83 more genes
    nsv4436307copy number variation1nstd102humanUncertain significance GRCh37 chr3: 4,403,157-4,599,731 , GRCh38.p12 chr3: 4,361,473-4,558,047 MRPS10P2, ITPR1-DT, 2 more genes
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