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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5890393copy number variation1nstd209human GRCh38 chr6: 32,184,580-32,184,642 , GRCh37.p13 chr6: 32,152,357-32,152,419 PBX2, AGER
    nsv5566913copy number variation1nstd207human GRCh38 chr6: 32,184,580-32,184,642 , GRCh37.p13 chr6: 32,152,357-32,152,419 PBX2, AGER
    nsv5473905copy number variation1nstd206human GRCh38 chr6: 32,184,584-32,184,643 , GRCh37.p13 chr6: 32,152,361-32,152,420 AGER, PBX2
    nsv5362819translocation1nstd200human GRCh38 chr6: 32,184,584-32,184,584 , GRCh38 chr6: 32,184,643-32,184,643 , GRCh37.p13 chr6: 32,152,361-32,152,361 , GRCh37.p13 chr6: 32,152,420-32,152,420 PBX2, AGER
    nsv5320521translocation1nstd204human GRCh37.p13 chr6: 32,152,361-32,152,361 , GRCh37.p13 chr6: 32,152,420-32,152,420 , GRCh38.p13 chr6: 32,184,584-32,184,584 , GRCh38.p13 chr6: 32,184,643-32,184,643 AGER, PBX2
    nsv5234405copy number variation1nstd204human GRCh38.p13 chr6: 30,240,001-32,313,700 , GRCh37.p13 chr6: 30,207,778-32,281,477 DDAH2, LOC105375018, 175 more genes
    nsv5231391copy number variation1nstd204human GRCh37.p13 chr6: 32,145,178-32,165,377 , GRCh38.p13 chr6: 32,177,401-32,197,600 AGER, NOTCH4, 5 more genes
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4675941copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055 AGER, AIF1, 217 more genes
    nsv4675453copy number variation1nstd102humanUncertain significance GRCh37 chr6: 31,916,915-32,278,000 , GRCh38.p12 chr6: 31,949,138-32,310,223 NOTCH4, CYP21A2, 29 more genes
    nsv4455450copy number variation1nstd102humanUncertain significance GRCh37 chr6: 32,027,371-32,448,599 , GRCh38.p12 chr6: 32,059,594-32,480,822 AGPAT1, HCG23, 23 more genes
    nsv4392308copy number variation1nstd171human GRCh37 chr6: 32,152,358-32,152,420 , GRCh38.p12 chr6: 32,184,581-32,184,643 AGER, PBX2
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv3967467copy number variation1nstd168human GRCh38 chr6: 32,182,974-32,219,798 , GRCh37.p13 chr6: 32,150,751-32,187,575 AGER, NOTCH4, 2 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3886007copy number variation1nstd102humanUncertain significance GRCh37 chr6: 31,952,482-32,243,155 , GRCh38.p12 chr6: 31,984,705-32,275,378 STK19B, NOTCH4, 22 more genes
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