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Items: 1 to 20 of 458

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148281copy number variation1nstd102humanPathogenic GRCh38 chr22: 49,757,859-50,740,457 , GRCh37.p13 chr22: 50,151,507-51,178,885 CHKB-CPT1B, ADM2, 49 more genes
    nsv7148150copy number variation1nstd102humanPathogenic GRCh37 chr22: 50,014,114-51,244,066 , GRCh38.p12 chr22: 49,620,466-50,805,638 MAPK11, KLHDC7B-DT, 54 more genes
    nsv7137656insertion1nstd232human GRCh37.p13 chr22: 50,651,112-50,651,112 , GRCh38.p12 chr22: 50,212,683-50,212,683 SELENOO
    nsv7096359copy number variation1nstd102humanUncertain significance GRCh37 chr22: 50,656,165-50,663,041 , GRCh38.p12 chr22: 50,217,736-50,224,612 SELENOO, TUBGCP6
    nsv7096316copy number variation1nstd102humanPathogenic GRCh37 chr22: 50,297,486-51,066,207 , GRCh38.p12 chr22: 49,903,838-50,627,779 RN7SL500P, DENND6B, 39 more genes
    nsv7074055inversion1nstd229human GRCh38 chr22: 50,153,100-50,445,127 , GRCh37.p13 chr22: 50,591,529-50,883,556 MOV10L1, PPP6R2, 14 more genes
    nsv7072051inversion1nstd229human GRCh38 chr22: 50,113,931-50,539,094 , GRCh37.p13 chr22: 50,552,360-50,977,523 NCAPH2, PPP6R2, 21 more genes
    nsv7059794inversion1nstd229human GRCh38 chr22: 50,156,227-50,492,045 , GRCh37.p13 chr22: 50,594,656-50,930,474 ADM2, PLXNB2, 16 more genes
    nsv7033075copy number variation1nstd229human GRCh38 chr22: 49,877,724-50,553,749 , GRCh37.p13 chr22: 50,271,372-50,992,178 SELENOO-AS1, MOV10L1, 33 more genes
    nsv7032952copy number variation1nstd229human GRCh38 chr22: 50,203,422-50,230,501 , GRCh37.p13 chr22: 50,641,851-50,668,930 SELENOO, SELENOO-AS1, 1 more genes
    nsv7032761copy number variation1nstd229human GRCh38 chr22: 50,193,309-50,287,205 , GRCh37.p13 chr22: 50,631,738-50,725,634 MAPK12, TUBGCP6, 6 more genes
    nsv7031449copy number variation1nstd229human GRCh38 chr22: 50,006,398-50,235,771 , GRCh37.p13 chr22: 50,444,827-50,674,200 PANX2, SELENOO-AS1, 7 more genes
    nsv7030124copy number variation1nstd229human GRCh38 chr22: 50,213,466-50,213,522 , GRCh37.p13 chr22: 50,651,895-50,651,951 SELENOO
    nsv7029202copy number variation1nstd229human GRCh38 chr22: 50,170,801-50,312,400 , GRCh37.p13 chr22: 50,609,230-50,750,829 MAPK12, TUBGCP6, 8 more genes
    nsv7027535copy number variation1nstd229human GRCh38 chr22: 50,153,101-50,218,800 , GRCh37.p13 chr22: 50,591,530-50,657,229 TUBGCP6, MOV10L1, 4 more genes
    nsv7022632copy number variation1nstd229human GRCh38 chr22: 50,209,189-50,209,907 , GRCh37.p13 chr22: 50,647,618-50,648,336 SELENOO-AS1, SELENOO
    nsv7020867copy number variation1nstd229human GRCh38 chr22: 50,210,328-50,255,070 , GRCh37.p13 chr22: 50,648,757-50,693,499 TUBGCP6, MAPK12, 3 more genes
    nsv6638073copy number variation1nstd102humanPathogenic GRCh37 chr22: 43,436,847-51,188,164 , GRCh38.p12 chr22: 43,040,841-50,749,736 SCUBE1-AS1, MIR6821, 165 more genes
    nsv6638067copy number variation1nstd102humanUncertain significance GRCh37 chr22: 50,636,593-50,736,663 , GRCh38.p12 chr22: 50,198,164-50,298,234 PLXNB2, SELENOO, 6 more genes
    nsv6637969copy number variation1nstd102humanPathogenic GRCh37 chr22: 44,178,749-51,183,840 , GRCh38.p12 chr22: 43,782,869-50,745,412 LOC105373081, RPL35AP36, 148 more genes
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