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Variant : CV382945 (GRCh37/hg19 10p15.3-11.23(chr10:100026-30278548)x3) Homo sapiens

Symbol: CV382945
Name: GRCh37/hg19 10p15.3-11.23(chr10:100026-30278548)x3
Condition: See cases [RCV000447131]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ABI1   ACBD5   ACBD7   ADARB2   AKR1C1   AKR1C2   AKR1C3   AKR1C4   AKR1E2   ANKRD16   ANKRD26   APBB1IP   ARHGAP21   ARL5B   ARMC3   ASB13   ATP5F1C   BAMBI   BEND7   BMI1   C10orf126   C10orf67   C1QL3   CACNB2   CALML3   CALML3-AS1   CALML5   CAMK1D   CCDC3   CDC123   CDNF   CELF2   COMMD3   COMMD3-BMI1   CUBN   DCLRE1C   DHTKD1   DIP2C   DNAJC1   EBLN1   ECHDC3   ENKUR   FAM107B   FAM171A1   FBH1   FRMD4A   GAD2   GATA3   GDI2   GPR158   GTPBP4   HACD1   HSPA14   IDI1   IDI2   IL15RA   IL2RA   ITGA8   ITIH2   ITIH5   KIAA1217   KIN   KLF6   LARP4B   LYZL1   MASTL   MCM10   MEIG1   MINDY3   MIR1915   MIR1915HG   MKX   MLLT10   MPP7   MSRB2   MYO3A   NEBL   NET1   NMT2   NSUN6   NUDT5   ODAD2   OLAH   OPTN   OTUD1   PDSS1   PFKFB3   PFKP   PHYH   PIP4K2A   PITRM1   PLXDC2   PRINS   PRKCQ   PROSER2   PRPF18   PRTFDC1   PTCHD3   PTER   PTF1A   RAB18   RBM17   RPP38   RPP38-DT   RSU1   SEC61A2   SEPHS1   SFMBT2   SKIDA1   SLC39A12   SPAG6   ST8SIA6   STAM   SUV39H2   SVIL   TAF3   TASOR2   THNSL1   TRDMT1   TUBAL3   UCMA   UCN3   UPF2   USP6NL   VIM   WAC   WDR37   YME1L1   ZMYND11  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3710100,026 - 30,278,548CLINVAR
Cytogenetic Map1010p15.3-11.23CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12851849
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-11-17
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.