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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7078067inversion1nstd229human GRCh38 chr22: 30,287,061-38,012,264 , GRCh37.p13 chr22: 30,683,050-38,408,271 LINC02885, RN7SL20P, 203 more genes
    nsv7076950inversion1nstd229human GRCh38 chr22: 30,591,076-30,599,163 , GRCh37.p13 chr22: 30,987,063-30,995,150 PES1
    nsv7075608inversion1nstd229human GRCh38 chr22: 30,571,710-30,574,815 , GRCh37.p13 chr22: 30,967,697-30,970,802 PES1, GAL3ST1
    nsv7068065inversion1nstd229human GRCh38 chr22: 27,585,838-32,538,391 , GRCh37.p13 chr22: 27,981,799-32,934,377 LOC105372995, NEFH, 147 more genes
    nsv7065500inversion1nstd229human GRCh38 chr22: 29,260,563-37,652,385 , GRCh37.p13 chr22: 29,656,552-38,048,392 RFPL1, PATZ1, 217 more genes
    nsv7037708copy number variation1nstd229human GRCh38 chr22: 30,596,344-30,600,883 , GRCh37.p13 chr22: 30,992,331-30,996,870 PES1
    nsv7035800copy number variation1nstd229human GRCh38 chr22: 30,480,363-30,697,469 , GRCh37.p13 chr22: 30,876,350-31,093,456 SIRPAP1, DUSP18, 10 more genes
    nsv7035348copy number variation1nstd229human GRCh38 chr22: 30,589,690-30,589,741 , GRCh37.p13 chr22: 30,985,677-30,985,728 PES1
    nsv7034649copy number variation1nstd229human GRCh38 chr22: 30,604,307-30,605,558 , GRCh37.p13 chr22: 31,000,294-31,001,545 PES1, TCN2
    nsv7033844copy number variation1nstd229human GRCh38 chr22: 30,592,544-30,600,318 , GRCh37.p13 chr22: 30,988,531-30,996,305 PES1
    nsv7031681copy number variation1nstd229human GRCh38 chr22: 30,592,063-30,633,192 , GRCh37.p13 chr22: 30,988,050-31,029,179 PES1, TCN2, 1 more genes
    nsv6638056copy number variation1nstd102humanUncertain significance GRCh37 chr22: 30,649,178-31,035,087 , GRCh38.p12 chr22: 30,253,189-30,639,100 GAL3ST1, SDC4P, 22 more genes
    nsv6553995copy number variation1nstd223human GRCh38 chr22: 30,597,987-30,603,003 , GRCh37.p13 chr22: 30,993,974-30,998,990 PES1
    nsv6548759copy number variation1nstd223human GRCh38 chr22: 30,598,901-30,601,400 , GRCh37.p13 chr22: 30,994,888-30,997,387 PES1
    nsv6538892copy number variation1nstd223human GRCh38 chr22: 30,589,601-30,591,100 , GRCh37.p13 chr22: 30,985,588-30,987,087 PES1
    nsv6311263copy number variation1nstd102humanUncertain significance GRCh37 chr22: 29,083,885-34,046,674 , GRCh38.p12 chr22: 28,687,897-33,650,688 SNORD125, LOC107985533, 145 more genes
    nsv6311183copy number variation1nstd102humanPathogenic GRCh37 chr22: 31,003,319-31,022,508 , GRCh38.p12 chr22: 30,607,332-30,626,521 TCN2, PES1
    nsv6252073mobile element insertion1nstd215human GRCh38 chr22: 30,602,450-30,602,450 , GRCh37.p13 chr22: 30,998,437-30,998,437 PES1
    nsv6252072mobile element insertion1nstd215human GRCh38 chr22: 30,597,896-30,597,896 , GRCh37.p13 chr22: 30,993,883-30,993,883 PES1
    nsv6213138copy number variation1nstd214human GRCh38 chr22: 30,589,688-30,589,740 , GRCh37.p13 chr22: 30,985,675-30,985,727 PES1
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