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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5902904copy number variation1nstd209human GRCh38 chr3: 66,803,410-74,489,186 , GRCh37.p13 chr3: 66,853,834-74,538,337 , LOC105377160, 83 more genes
    nsv5836786copy number variation1nstd209human GRCh38 chr3: 71,756,537-71,758,386 , GRCh37.p13 chr3: 71,805,688-71,807,537 GPR27
    nsv5564432copy number variation1nstd102humanPathogenic GRCh37 chr3: 68,939,251-72,700,418 , GRCh38.p12 chr3: 68,890,100-72,651,267 CCDC137P1, LOC105377160, 39 more genes
    nsv5227729copy number variation1nstd204human GRCh38.p13 chr3: 71,752,201-71,754,900 , GRCh37.p13 chr3: 71,801,352-71,804,051 GPR27, EIF4E3
    nsv5033386inversion1nstd200human GRCh38 chr3: 66,830,019-82,426,887 , GRCh37.p13 chr3: 66,880,443-82,476,038 , HNRNPA3P6, 150 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    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
    nsv4728221copy number variation1nstd102humanUncertain significance GRCh37 chr3: 70,938,608-74,660,846 , GRCh38.p12 chr3: 70,889,457-74,611,695 CCDC137P1, LINC02047, 45 more genes
    nsv4674193copy number variation1nstd102humanUncertain significance GRCh37 chr3: 71,665,558-72,020,026 , GRCh38.p12 chr3: 71,616,407-71,970,875 PROK2, LOC105377156, 4 more genes
    nsv4596610copy number variation1nstd183human GRCh37 chr3: 71,802,926-71,805,413 , GRCh38.p12 chr3: 71,753,775-71,756,262 EIF4E3, GPR27
    nsv4586679copy number variation1nstd183human GRCh37 chr3: 71,802,175-71,804,230 , GRCh38.p12 chr3: 71,753,024-71,755,079 GPR27, EIF4E3
    nsv4586593copy number variation1nstd183human GRCh37 chr3: 71,802,926-71,802,971 , GRCh38.p12 chr3: 71,753,775-71,753,820 EIF4E3, GPR27
    nsv4586592copy number variation1nstd183human GRCh37 chr3: 71,802,284-71,804,379 , GRCh38.p12 chr3: 71,753,133-71,755,228 GPR27, EIF4E3
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4405763copy number variation1nstd174human GRCh37 chr3: 71,801,712-71,804,230 , GRCh38.p12 chr3: 71,752,561-71,755,079 GPR27, EIF4E3
    nsv4405554copy number variation1nstd174human GRCh37 chr3: 71,803,052-71,804,456 , GRCh38.p12 chr3: 71,753,901-71,755,305 GPR27, EIF4E3
    nsv3955303copy number variation1nstd168human GRCh38 chr3: 71,744,124-71,809,777 , GRCh37.p13 chr3: 71,793,275-71,858,928 PROK2, EIF4E3, 2 more genes
    nsv3924472copy number variation1nstd102humanUncertain significance NCBI36 chr3: 71,256,348-72,024,108 , GRCh37 chr3: 71,173,658-71,941,418 , GRCh38 chr3: 71,124,507-71,892,267 MIR1284, RN7SL271P, 7 more genes
    nsv3922768copy number variation1nstd102humanPathogenic GRCh37 chr3: 64,746,924-78,459,248 , GRCh38 chr3: 64,761,248-78,410,098 , NCBI36 chr3: 64,721,964-78,541,938 RNU6-557P, LOC105377160, 147 more genes
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