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Items: 1 to 20 of 109

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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
    nsv7074963inversion1nstd229human GRCh38 chr22: 31,201,802-31,493,198 , GRCh37.p13 chr22: 31,597,788-31,889,184 PPP1R14BP1, PIK3IP1, 12 more genes
    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
    nsv7023728copy number variation1nstd229human GRCh38 chr22: 31,349,044-31,349,085 , GRCh37.p13 chr22: 31,745,030-31,745,071 LINC01521
    nsv7020405copy number variation1nstd229human GRCh38 chr22: 31,348,280-31,358,197 , GRCh37.p13 chr22: 31,744,266-31,754,183 LINC01521
    nsv6548421copy number variation1nstd223human GRCh38 chr22: 31,348,001-31,603,200 , GRCh37.p13 chr22: 31,743,987-31,999,186 LINC01521, DRG1, 6 more genes
    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
    nsv6134210copy number variation1nstd213human GRCh37 chr22: 30,130,000-36,350,001 , GRCh38.p12 chr22: 29,734,011-35,953,953 HMOX1, LIF, 146 more genes
    nsv6134118copy number variation1nstd213human GRCh37 chr22: 27,870,000-35,640,001 , GRCh38.p12 chr22: 27,474,039-35,244,008 AP1B1, EWSR1, 172 more genes
    nsv5550017copy number variation1nstd206human GRCh38 chr22: 31,351,515-31,354,111 , GRCh37.p13 chr22: 31,747,501-31,750,097 LINC01521
    nsv5032926copy number variation1nstd200human GRCh38 chr22: 31,348,280-31,358,168 , GRCh37.p13 chr22: 31,744,266-31,754,154 LINC01521
    nsv4729980copy number variation1nstd102humanUncertain significance GRCh37 chr22: 31,565,901-32,105,115 , GRCh38.p12 chr22: 31,169,915-31,709,129 LINC01521, RNU6-338P, 18 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
    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
    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
    nsv4282425copy number variation1nstd166human GRCh37.p13 chr22: 31,744,250-31,744,365 , GRCh38.p12 chr22: 31,348,264-31,348,379 LINC01521
    nsv4281943copy number variation1nstd166human GRCh37.p13 chr22: 31,744,266-31,754,154 , GRCh38.p12 chr22: 31,348,280-31,358,168 LINC01521
    nsv4273009copy number variation1nstd166human GRCh37.p13 chr22: 31,743,516-31,752,853 , GRCh38.p12 chr22: 31,347,530-31,356,867 LINC01521
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