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Items: 1 to 20 of 136

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5718417mobile element insertion1nstd211human GRCh38 chr22: 37,657,716-37,657,716 , GRCh37.p13 chr22: 38,053,723-38,053,723 PDXP, PDXP-DT
    nsv5671951insertion1nstd207human GRCh38 chr22: 37,656,829-37,656,829 , GRCh37.p13 chr22: 38,052,836-38,052,836 PDXP-DT, PDXP
    nsv5554043mobile element insertion1nstd206human GRCh38 chr22: 37,657,730-37,657,767 , GRCh37.p13 chr22: 38,053,737-38,053,774 PDXP-DT, PDXP
    nsv5365738translocation1nstd200human GRCh38 chr17: 5,056,428-5,056,428 , GRCh38 chr22: 37,657,730-37,657,730 , GRCh37.p13 chr22: 38,053,737-38,053,737 , GRCh37.p13 chr17: 4,959,723-4,959,723 PDXP-DT, PDXP
    nsv5186191mobile element insertion1nstd203human GRCh38 chr22: 37,657,715-37,657,715 , GRCh37.p13 chr22: 38,053,722-38,053,722 PDXP-DT, PDXP
    nsv5179236mobile element insertion1nstd203human GRCh38 chr22: 37,657,715-37,657,730 , GRCh37.p13 chr22: 38,053,722-38,053,737 PDXP, PDXP-DT
    nsv5177018mobile element insertion1nstd203human GRCh38 chr22: 37,656,829-37,656,834 , GRCh37.p13 chr22: 38,052,836-38,052,841 PDXP-DT, PDXP
    nsv5174970mobile element insertion1nstd203human GRCh38 chr22: 37,656,826-37,656,834 , GRCh37.p13 chr22: 38,052,833-38,052,841 PDXP, PDXP-DT
    nsv5173823mobile element insertion1nstd203human GRCh38 chr22: 37,656,827-37,656,834 , GRCh37.p13 chr22: 38,052,834-38,052,841 PDXP-DT, PDXP
    nsv5173815mobile element insertion1nstd203human GRCh38 chr22: 37,657,716-37,657,730 , GRCh37.p13 chr22: 38,053,723-38,053,737 PDXP, PDXP-DT
    nsv5171850mobile element insertion1nstd203human GRCh38 chr22: 37,656,830-37,656,834 , GRCh37.p13 chr22: 38,052,837-38,052,841 PDXP, PDXP-DT
    nsv5171114mobile element insertion1nstd203human GRCh38 chr22: 37,656,831-37,656,840 , GRCh37.p13 chr22: 38,052,838-38,052,847 PDXP, PDXP-DT
    nsv5168659mobile element insertion1nstd203human GRCh38 chr22: 37,656,832-37,656,834 , GRCh37.p13 chr22: 38,052,839-38,052,841 PDXP-DT, PDXP
    nsv5161298mobile element insertion1nstd203human GRCh38 chr22: 37,657,721-37,657,730 , GRCh37.p13 chr22: 38,053,728-38,053,737 PDXP, PDXP-DT
    nsv5038058copy number variation1nstd200human GRCh38 chr22: 37,638,954-37,645,626 , GRCh37.p13 chr22: 38,034,961-38,041,633 PDXP-DT, SH3BP1
    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
    nsv4676116copy number variation1nstd102humanPathogenic GRCh37 chr22: 38,002,218-38,973,070 , GRCh38.p12 chr22: 37,606,211-38,577,065 CSNK1E, RN7SL704P, 43 more genes
    nsv4633240copy number variation1nstd183human GRCh37 chr22: 38,054,434-38,055,177 , GRCh38.p12 chr22: 37,658,427-37,659,170 PDXP, PDXP-DT
    nsv4573545mobile element insertion1nstd166human GRCh37.p13 chr22: 38,053,723-38,053,723 , GRCh38.p12 chr22: 37,657,716-37,657,716 PDXP, PDXP-DT
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