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Items: 1 to 20 of 205

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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
    nsv5686285mobile element insertion1nstd211human GRCh38 chr3: 5,198,684-5,198,684 , GRCh37.p13 chr3: 5,240,369-5,240,369 EDEM1
    nsv5448116copy number variation1nstd206human GRCh38 chr3: 5,190,803-5,191,656 , GRCh37.p13 chr3: 5,232,488-5,233,341 EDEM1
    nsv5445946copy number variation1nstd206human GRCh38 chr3: 5,202,229-5,202,376 , GRCh37.p13 chr3: 5,243,914-5,244,061 EDEM1
    nsv5441779copy number variation1nstd206human GRCh38 chr3: 4,977,918-5,188,644 , GRCh37.p13 chr3: 5,019,603-5,230,329 , BHLHE40, 5 more genes
    nsv5438116copy number variation1nstd206human GRCh38 chr3: 5,212,836-5,212,927 , GRCh37.p13 chr3: 5,254,521-5,254,612 EDEM1
    nsv5381423copy number variation1nstd102humanPathogenic GRCh37 chr3: 73,914-5,940,479 , GRCh38.p12 chr3: 32,241-5,898,792 ITPR1-DT, RPSAP32, 54 more genes
    nsv5198920mobile element insertion1nstd203human GRCh38 chr3: 5,190,865-5,190,878 , GRCh37.p13 chr3: 5,232,550-5,232,563 EDEM1
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4917508copy number variation1nstd200human GRCh38 chr3: 5,189,886-5,200,174 , GRCh37.p13 chr3: 5,231,571-5,241,859 EDEM1
    nsv4917507copy number variation1nstd200human GRCh38 chr3: 5,186,980-5,187,106 , GRCh37.p13 chr3: 5,228,665-5,228,791 EDEM1
    nsv4917506copy number variation1nstd200human GRCh38 chr3: 5,183,042-5,186,523 , GRCh37.p13 chr3: 5,224,727-5,228,208 EDEM1
    nsv4914278copy number variation1nstd200human GRCh38 chr3: 5,200,167-5,422,074 , GRCh37.p13 chr3: 5,241,852-5,463,760 EDEM1, MIR4790, 1 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4796085copy number variation1nstd200human GRCh37 chr3: 5,231,571-5,241,859 , GRCh38.p12 chr3: 5,189,886-5,200,174 EDEM1
    nsv4728681copy number variation1nstd102humanUncertain significance GRCh37 chr3: 4,921,390-5,408,983 , GRCh38.p12 chr3: 4,879,706-5,367,298 RN7SL553P, BHLHE40-AS1, 6 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
    nsv4664220copy number variation1nstd186human GRCh37 chr3: 5,229,554-5,230,367 , GRCh38.p12 chr3: 5,187,869-5,188,682 EDEM1
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