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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979701insertion1nstd209human GRCh38 chr22: 30,966,105-30,966,105 , GRCh37.p13 chr22: 31,362,091-31,362,091 MORC2
    nsv5876053copy number variation1nstd209human GRCh38 chr22: 30,954,648-30,955,650 , GRCh37.p13 chr22: 31,350,634-31,351,636 MORC2
    nsv5161675mobile element insertion1nstd203human GRCh38 chr22: 30,929,214-30,929,229 , GRCh37.p13 chr22: 31,325,201-31,325,216 MORC2
    nsv5036260copy number variation1nstd200human GRCh38 chr22: 30,938,696-30,938,816 , GRCh37.p13 chr22: 31,334,683-31,334,803 MORC2
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4676292copy number variation1nstd102humanPathogenic GRCh37 chr22: 30,654,764-51,197,838 , GRCh38.p12 chr22: 30,258,775-50,759,410 PDXP-DT, PDGFB, 550 more genes
    nsv4575521mobile element insertion1nstd166human GRCh37.p13 chr22: 31,331,833-31,331,833 , GRCh38.p12 chr22: 30,935,846-30,935,846 MORC2
    nsv4508093mobile element insertion1nstd166human GRCh37.p13 chr22: 31,325,201-31,325,201 , GRCh38.p12 chr22: 30,929,214-30,929,214 MORC2
    nsv4457771copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410 IGLV3-27, XKR3, 1082 more genes
    nsv4436827inversion1nstd102humanLikely pathogenic GRCh38.p12 chr22: 29,288,727-31,344,669 , GRCh37 chr22: 29,684,716-31,740,655 AP1B1, EWSR1, 81 more genes
    nsv4383389copy number variation1nstd173human GRCh37 chr22: 21,465,662-33,984,045 , GRCh38.p12 chr22: 21,111,373-33,588,059 , XBP1, 450 more genes
    nsv4284347copy number variation1nstd166human GRCh37.p13 chr22: 31,332,852-31,334,373 , GRCh38.p12 chr22: 30,936,865-30,938,386 MORC2
    nsv4277452copy number variation1nstd166human GRCh37.p13 chr22: 31,318,049-31,319,996 , GRCh38.p12 chr22: 30,922,062-30,924,009 MORC2-AS1, MORC2, 1 more genes
    nsv4275573copy number variation1nstd166human GRCh37.p13 chr22: 31,358,115-31,358,198 , GRCh38.p12 chr22: 30,962,129-30,962,212 MORC2
    nsv4275529copy number variation1nstd166human GRCh37.p13 chr22: 31,322,552-31,325,193 , GRCh38.p12 chr22: 30,926,565-30,929,206 MORC2, MORC2-AS1
    nsv3923324copy number variation1nstd102humanUncertain significance NCBI36 chr22: 29,038,245-29,676,302 , GRCh37 chr22: 30,708,245-31,346,302 , GRCh38 chr22: 30,312,256-30,950,316 SLC35E4, OSBP2, 28 more genes
    nsv3923205copy number variation1nstd102humanPathogenic NCBI36 chr22: 25,177,008-30,177,912 , GRCh37 chr22: 26,847,008-31,847,912 , GRCh38 chr22: 26,451,042-31,451,926 DRG1, THOC5, 138 more genes
    nsv3922708copy number variation1nstd102humanPathogenic GRCh38 chr22: 23,279,231-36,247,369 , GRCh37 chr22: 23,621,418-36,643,415 , NCBI36 chr22: 21,951,418-34,973,361 DRICH1, MMP11, 316 more genes
    nsv3919881copy number variation1nstd102humanPathogenic GRCh37 chr22: 17,397,633-51,178,213 , GRCh38 chr22: 16,916,743-50,739,785 , NCBI36 chr22: 15,777,633-49,525,079 MIR12114, MIR6820, 1059 more genes
    nsv3919429copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,661,724-32,217,179 , GRCh38 chr22: 18,178,957-31,821,193 , NCBI36 chr22: 17,041,724-30,547,179 PCAT14, MIR3199-1, 533 more genes
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