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Items: 1 to 20 of 136

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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
    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
    nsv4924153copy number variation1nstd200human GRCh38 chr3: 6,728,898-6,846,348 , GRCh37.p13 chr3: 6,770,585-6,888,035 LOC105376944, MRPS36P1, 3 more genes
    nsv4924152copy number variation1nstd200human GRCh38 chr3: 6,646,662-6,783,183 , GRCh37.p13 chr3: 6,688,349-6,824,870 GRM7-AS3, LOC105376943, 2 more genes
    nsv4924147copy number variation1nstd200human GRCh38 chr3: 5,914,186-6,794,931 , GRCh37.p13 chr3: 5,955,873-6,836,618 LOC102723596, LOC105376944, 4 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4793823copy number variation1nstd200human GRCh37 chr3: 5,955,873-6,836,618 , GRCh38.p12 chr3: 5,914,186-6,794,931 LOC102723596, LOC105376944, 4 more genes
    nsv4728354copy number variation1nstd102humanUncertain significance GRCh37 chr3: 6,124,359-7,091,641 , GRCh38.p12 chr3: 6,082,672-7,049,954 GRM7-AS2, LOC105376943, 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
    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
    nsv4453673copy number variation2nstd102humanUncertain significance GRCh37 chr3: 6,120,068-7,991,449 , GRCh38.p12 chr3: 6,078,381-7,949,762 GRM7, LOC105376942, 7 more genes
    nsv4452943copy number variation1nstd102humanUncertain significance GRCh37 chr3: 5,492,215-7,221,271 , GRCh38.p12 chr3: 5,450,529-7,179,584 LOC105376939, LOC105376940, 11 more genes
    nsv4452537copy number variation1nstd102humanUncertain significance GRCh37 chr3: 6,206,633-6,981,500 , GRCh38.p12 chr3: 6,164,946-6,939,813 GRM7-AS2, GRM7, 6 more genes
    nsv4451599copy number variation1nstd102humanUncertain significance GRCh37 chr3: 5,163,462-7,925,439 , GRCh38.p12 chr3: 5,121,777-7,883,752 MIR4790, LOC105376938, 18 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
    nsv4436544copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 36,016-9,307,855 , GRCh38.p12 chr3: 18,324-9,266,171 CAV3, GRM7, 83 more genes
    nsv4400828copy number variation1nstd174human GRCh37 chr3: 6,749,470-7,586,275 , GRCh38.p12 chr3: 6,707,783-7,544,588 GRM7, MRPS36P1, 6 more genes
    nsv4365525copy number variation1nstd173human GRCh37 chr3: 5,487,436-7,225,364 , GRCh38.p12 chr3: 5,445,750-7,183,677 LOC105376940, LOC105376943, 12 more genes
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