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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5722278mobile element insertion1nstd211human GRCh38 chr22: 32,484,716-32,484,716 , GRCh37.p13 chr22: 32,880,703-32,880,703 FBXO7
    nsv5703664mobile element insertion1nstd211human GRCh38 chr22: 32,482,493-32,482,493 , GRCh37.p13 chr22: 32,878,480-32,878,480 FBXO7
    nsv5590136copy number variation1nstd207human GRCh38 chr22: 32,491,562-32,491,619 , GRCh37.p13 chr22: 32,887,549-32,887,606 FBXO7
    nsv5417449mobile element insertion1nstd206human GRCh38 chr22: 32,482,493-32,482,544 , GRCh37.p13 chr22: 32,878,480-32,878,531 FBXO7
    nsv5355468translocation1nstd200human GRCh38 chr22: 32,476,677-32,476,677 , GRCh38 chr11: 102,110,637-102,110,637 , GRCh37.p13 chr11: 101,981,368-101,981,368 , GRCh37.p13 chr22: 32,872,664-32,872,664 YAP1, FBXO7
    nsv5199048mobile element insertion1nstd203human GRCh38 chr22: 32,473,253-32,473,270 , GRCh37.p13 chr22: 32,869,240-32,869,257 FBXO7
    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
    nsv4622057copy number variation1nstd183human GRCh37 chr22: 32,891,439-32,891,749 , GRCh38.p12 chr22: 32,495,452-32,495,762 FBXO7
    nsv4568112mobile element insertion1nstd166human GRCh37.p13 chr22: 32,890,785-32,890,785 , GRCh38.p12 chr22: 32,494,798-32,494,798 FBXO7
    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
    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
    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
    nsv3915130copy number variation1nstd102humanPathogenic GRCh38 chr22: 26,979,579-33,992,220 , NCBI36 chr22: 25,705,542-32,718,209 , GRCh37 chr22: 27,375,542-34,388,209 TIMP3, MIR7109, 170 more genes
    nsv3914617copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,261,514-37,583,387 , GRCh38 chr22: 20,907,226-37,187,347 , NCBI36 chr22: 19,591,514-35,913,333 RASL10A, SNORD125, 525 more genes
    nsv3913775copy number variation1nstd102humanPathogenic NCBI36 chr22: 15,777,498-49,525,130 , GRCh38 chr22: 16,916,608-50,739,836 , GRCh37 chr22: 17,397,498-51,178,264 ZNF280A, RFPL1S, 1059 more genes
    nsv3907231copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,114,244-51,211,392 , GRCh38.p12 chr22: 16,367,190-50,772,964 DDTL, PPP1R26P3, 1084 more genes
    nsv3902776copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,054,667-51,243,435 , GRCh38.p12 chr22: 16,367,190-50,805,007 LOC100419811, MTCO2P20, 1084 more genes
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