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Items: 1 to 20 of 148

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5888582copy number variation1nstd209human GRCh38 chr3: 46,802,705-48,210,414 , GRCh37.p13 chr3: 46,844,195-48,251,904 SNORD13P3, LOC105377074, 34 more genes
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 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
    nsv4924399copy number variation1nstd200human GRCh38 chr3: 47,377,408-47,386,339 , GRCh37.p13 chr3: 47,418,898-47,427,829 PTPN23
    nsv4924397copy number variation1nstd200human GRCh38 chr3: 47,344,940-47,923,420 , GRCh37.p13 chr3: 47,386,430-47,964,910 PTPN23, DHX30, 13 more genes
    nsv4924396copy number variation1nstd200human GRCh38 chr3: 47,223,435-47,451,677 , GRCh37.p13 chr3: 47,264,925-47,493,167 KLHL18, PTPN23, 5 more genes
    nsv4911150copy number variation1nstd200human GRCh38 chr3: 47,402,252-47,408,739 , GRCh37.p13 chr3: 47,443,742-47,450,229 PTPN23
    nsv4911149copy number variation1nstd200human GRCh38 chr3: 47,356,985-47,379,456 , GRCh37.p13 chr3: 47,398,475-47,420,946 PTPN23
    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
    nsv4790559copy number variation1nstd200human GRCh37 chr3: 47,446,933-47,447,025 , GRCh38.p12 chr3: 47,405,443-47,405,535 PTPN23
    nsv4596493copy number variation1nstd183human GRCh37 chr3: 47,450,672-47,451,209 , GRCh38.p12 chr3: 47,409,182-47,409,719 PTPN23
    nsv4588739copy number variation1nstd183human GRCh37 chr3: 47,450,973-47,451,217 , GRCh38.p12 chr3: 47,409,483-47,409,727 PTPN23
    nsv4586270copy number variation1nstd183human GRCh37 chr3: 47,450,973-47,451,020 , GRCh38.p12 chr3: 47,409,483-47,409,530 PTPN23
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4453008copy number variation1nstd102humanUncertain significance GRCh37 chr3: 47,068,320-47,472,020 , GRCh38.p12 chr3: 47,026,830-47,430,530 SCAP, SETD2, 7 more genes
    nsv4347762copy number variation1nstd102humanPathogenic GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589 UQCRC1, DHX30, 291 more genes
    nsv4084135copy number variation1nstd166human GRCh37.p13 chr3: 47,329,656-47,494,755 , GRCh38.p12 chr3: 47,288,166-47,453,265 PTPN23, SCAP, 1 more genes
    nsv4077543copy number variation1nstd166human GRCh37.p13 chr3: 47,424,134-47,424,215 , GRCh38.p12 chr3: 47,382,644-47,382,725 PTPN23
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