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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950605insertion1nstd209human GRCh38 chr3: 63,203,061-63,203,061 , GRCh37.p13 chr3: 63,188,737-63,188,737 SYNPR, UBL5P3
    nsv5436808copy number variation1nstd206human GRCh38 chr3: 62,956,000-63,216,000 , GRCh37.p13 chr3: 62,941,675-63,201,676 , SYNPR, 3 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4918597copy number variation1nstd200human GRCh38 chr3: 63,171,953-63,203,102 , GRCh37.p13 chr3: 63,157,629-63,188,778 SYNPR, UBL5P3
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4796806copy number variation1nstd200human GRCh37 chr3: 63,157,629-63,188,778 , GRCh38.p12 chr3: 63,171,953-63,203,102 UBL5P3, SYNPR
    nsv4728543copy number variation1nstd102humanUncertain significance GRCh37 chr3: 62,894,703-63,320,384 , GRCh38.p12 chr3: 62,909,028-63,334,708 UBL5P3, SYNPR, 3 more genes
    nsv4685651copy number variation1nstd102humanUncertain significance GRCh37 chr3: 62,899,731-63,601,696 , GRCh38.p12 chr3: 62,914,056-63,616,020 KRT8P35, RPS10P10, 5 more genes
    nsv4678912copy number variation1nstd189human GRCh37.p13 chr3: 62,866,394-63,588,304 , GRCh38.p12 chr3: 62,880,719-63,602,628 , SYNPR, 6 more genes
    nsv4674813copy number variation1nstd102humanUncertain significance GRCh37 chr3: 62,206,958-63,944,889 , GRCh38.p12 chr3: 62,221,284-63,959,213 RNA5SP134, LOC105377647, 22 more genes
    nsv4674306copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,449,667-65,561,638 , GRCh38.p12 chr3: 60,463,934-65,575,963 THOC7-AS1, LOC105377647, 56 more genes
    nsv4588982copy number variation1nstd183human GRCh37 chr3: 63,166,748-63,187,995 , GRCh38.p12 chr3: 63,181,072-63,202,319 UBL5P3, SYNPR
    nsv4588981copy number variation1nstd183human GRCh37 chr3: 63,128,233-63,193,105 , GRCh38.p12 chr3: 63,142,557-63,207,429 , SYNPR, 1 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
    nsv4452524copy number variation1nstd102humanPathogenic GRCh37 chr3: 57,076,136-65,716,956 , GRCh38.p12 chr3: 57,042,108-65,731,281 LOC105377114, FAM107A, 110 more genes
    nsv4450340copy number variation1nstd102humanUncertain significance GRCh37 chr3: 60,844,727-63,983,596 , GRCh38.p12 chr3: 60,859,055-63,997,920 RNU2-10P, THOC7, 29 more genes
    nsv4395152copy number variation1nstd174human GRCh37 chr3: 62,861,850-63,196,657 , GRCh38.p12 chr3: 62,876,175-63,210,981 , CADPS, 5 more genes
    nsv4087753copy number variation1nstd166human GRCh37.p13 chr3: 63,039,190-63,205,089 , GRCh38.p12 chr3: 63,053,514-63,219,413 , SYNPR, 3 more genes
    nsv4073047copy number variation1nstd166human GRCh37.p13 chr3: 63,182,335-63,190,512 , GRCh38.p12 chr3: 63,196,659-63,204,836 UBL5P3, SYNPR
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