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Items: 1 to 20 of 83

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5381193copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,912,954-11,200,309 , GRCh38.p12 chr19: 10,802,278-11,089,633 SMARCA4, RN7SL192P, 10 more genes
    nsv5287330copy number variation1nstd204human GRCh38.p13 chr19: 10,335,601-11,755,400 , GRCh37.p13 chr19: 10,446,277-11,866,215 AP1M2, C19orf38, 64 more genes
    nsv5286584copy number variation1nstd204human GRCh37.p13 chr19: 10,844,077-10,981,976 , GRCh38.p13 chr19: 10,733,401-10,871,300 DNM2, CARM1, 5 more genes
    nsv4685775copy number variation1nstd102humannot provided GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253 SLC44A2, ZNF833P, 114 more genes
    nsv4676283copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,632,623-11,135,294 , GRCh38.p12 chr19: 10,521,947-11,024,618 ATG4D, RN7SL192P, 21 more genes
    nsv4628771copy number variation1nstd183human GRCh37 chr19: 10,788,813-10,988,086 , GRCh38.p12 chr19: 10,678,137-10,877,410 DNM2, CARM1, 8 more genes
    nsv4457721copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,441,330-10,977,962 , GRCh38.p12 chr19: 10,330,654-10,867,286 CDKN2D, QTRT1, 24 more genes
    nsv4451686copy number variation1nstd102humannot provided GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253 ODAD3, RNA5SP466, 114 more genes
    nsv4376309copy number variation1nstd173human GRCh37 chr19: 10,902,794-10,938,252 , GRCh38.p12 chr19: 10,792,118-10,827,576 MIR199A1, MIR6793, 1 more genes
    nsv4343662sequence alteration1nstd166human GRCh38.p12 chr19: 10,695,422-10,849,576 , GRCh37.p13 chr19: 10,806,098-10,960,252 DNM2, TMED1, 6 more genes
    nsv3923415copy number variation1nstd102humanPathogenic NCBI36 chr19: 10,286,934-14,020,806 , GRCh37 chr19: 10,425,934-14,159,806 , GRCh38 chr19: 10,315,258-14,048,994 MAN2B1, SWSAP1, 182 more genes
    nsv3922999copy number variation1nstd102humanPathogenic NCBI36 chr19: 10,240,071-12,946,266 , GRCh37.p13 chr19: 10,379,071-13,085,266 , GRCh38.p12 chr19: 10,268,395-12,974,452 ZNF433, MIR6794, 155 more genes
    nsv3922964copy number variation1nstd102humanPathogenic GRCh38 chr19: 10,319,474-13,777,860 , NCBI36 chr19: 10,291,150-13,749,674 , GRCh37 chr19: 10,430,150-13,888,674 SWSAP1, LOC105372284, 164 more genes
    nsv3922509copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 10,302,331-10,892,228 , GRCh37 chr19: 10,441,331-11,031,228 , GRCh38 chr19: 10,330,655-10,920,552 CDKN2D, DNM2, 26 more genes
    nsv3920643copy number variation1nstd102humanPathogenic GRCh37 chr19: 10,267,082-11,000,364 , NCBI36 chr19: 10,128,082-10,861,364 , GRCh38 chr19: 10,156,406-10,889,688 MIR4748, ZGLP1, 36 more genes
    nsv3920616copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 8,802,823-13,303,041 , GRCh37 chr19: 8,941,823-13,442,041 , GRCh38 chr19: 8,831,147-13,331,227 ACP5, GET3, 236 more genes
    nsv3912242copy number variation1nstd102humanPathogenic GRCh37 chr19: 9,846,119-11,338,677 , GRCh38 chr19: 9,735,443-11,228,001 , NCBI36 chr19: 9,707,119-11,199,677 PPAN, S1PR5, 68 more genes
    nsv3905293copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,584,393-10,938,252 , GRCh38.p12 chr19: 10,473,717-10,827,576 MIR638, AP1M2, 16 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
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