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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5883405copy number variation1nstd209human GRCh38 chr22: 24,766,507-24,769,372 , GRCh37.p13 chr22: 25,162,474-25,165,339 PIWIL3, TOP1P2
    nsv5878009copy number variation1nstd209human GRCh38 chr22: 24,766,307-24,767,706 , GRCh37.p13 chr22: 25,162,274-25,163,673 TOP1P2, PIWIL3
    nsv5033351copy number variation1nstd200human GRCh38 chr22: 24,718,940-24,767,986 , GRCh37.p13 chr22: 25,114,907-25,163,953 PIWIL3, TOP1P2
    nsv4768383copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-26,483,608 , GRCh38.p12 chr22: 16,408,173-26,087,642 KRT18P62, LOC101060852, 437 more genes
    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
    nsv4680763copy number variation1nstd189human GRCh37.p13 chr22: 24,891,356-26,623,160 , GRCh38.p12 chr22: 24,495,388-26,227,194 , GRK3, 37 more genes
    nsv4680353copy number variation1nstd189human GRCh37.p13 chr22: 25,013,443-25,483,921 , GRCh38.p12 chr22: 24,617,476-25,087,954 GGT1, TOP1P2, 10 more genes
    nsv4676422copy number variation1nstd102humanUncertain significance GRCh37 chr22: 24,311,474-26,075,188 , GRCh38.p12 chr22: 24,013,510-25,679,221 SPECC1L, LOC105372969, 39 more genes
    nsv4676211copy number variation1nstd102humanPathogenic GRCh37 chr22: 20,732,808-25,193,541 , GRCh38.p12 chr22: 20,378,518-24,797,574 IGLV3-16, ASH2LP2, 266 more genes
    nsv4676144copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-27,657,507 , GRCh38.p12 chr22: 16,408,173-27,261,546 LINC02891, IGLV4-69, 466 more genes
    nsv4621861copy number variation1nstd183human GRCh37 chr22: 25,102,007-25,246,398 , GRCh38.p12 chr22: 24,706,040-24,850,431 TOP1P2, PIWIL3, 3 more genes
    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
    nsv4383389copy number variation1nstd173human GRCh37 chr22: 21,465,662-33,984,045 , GRCh38.p12 chr22: 21,111,373-33,588,059 , XBP1, 450 more genes
    nsv4316382inversion1nstd166human GRCh37.p13 chr22: 22,466,414-30,881,792 , GRCh38.p12 chr22: 22,112,004-30,485,805 , CRYBB2, 313 more genes
    nsv4285000copy number variation1nstd166human GRCh37.p13 chr22: 25,122,290-25,318,511 , GRCh38.p12 chr22: 24,726,323-24,922,544 SGSM1, PIWIL3, 1 more genes
    nsv3922923copy number variation1nstd102humanUncertain significance NCBI36 chr22: 23,370,615-23,573,315 , GRCh37.p13 chr22: 25,040,615-25,243,315 , GRCh38.p12 chr22: 24,644,648-24,847,348 LOC105372962, ARL5AP4, 7 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
    nsv3919085copy number variation1nstd102humanPathogenic NCBI36 chr22: 17,008,132-49,591,432 , GRCh37.p13 chr22: 18,628,132-51,244,566 , GRCh38.p12 chr22: 18,145,365-50,806,138 IGLV2-28, LINC01310, 1023 more genes
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