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Variant : CV436922 (GRCh37/hg19 10p15.3-q11.23(chr10:100026-50961640)x3) Homo sapiens

Symbol: CV436922
Name: GRCh37/hg19 10p15.3-q11.23(chr10:100026-50961640)x3
Condition: See cases [RCV000510893]
Clinical Significance: pathogenic
Last Evaluated: 06/03/2014
Review Status: no assertion criteria provided
Related Genes: ABI1   ACBD5   ACBD7   ADARB2   AGAP4   AGAP9   AKR1C1   AKR1C2   AKR1C3   AKR1C4   AKR1E2   ALOX5   ANKRD16   ANKRD26   ANKRD30A   ANXA8   ANXA8L1   APBB1IP   ARHGAP12   ARHGAP21   ARHGAP22   ARL5B   ARMC3   ASB13   ATP5F1C   BAMBI   BEND7   BMI1   BMS1   C10orf126   C10orf53   C10orf67   C10orf71   C1QL3   CACNB2   CALML3   CALML3-AS1   CALML5   CAMK1D   CCDC3   CCDC7   CCNY   CDC123   CDNF   CELF2   CHAT   COMMD3   COMMD3-BMI1   CREM   CSGALNACT2   CUBN   CUL2   CXCL12   DCLRE1C   DEPP1   DHTKD1   DIP2C   DNAJC1   DRGX   EBLN1   ECHDC3   ENKUR   EPC1   ERCC6   FAM107B   FAM170B   FAM171A1   FAM25C   FAM25E   FAM25G   FBH1   FRMD4A   FRMPD2   FXYD4   FZD8   GAD2   GATA3   GDF10   GDF2   GDI2   GJD4   GPR158   GPRIN2   GTPBP4   HACD1   HNRNPF   HSPA14   IDI1   IDI2   IL15RA   IL2RA   ITGA8   ITGB1   ITIH2   ITIH5   JCAD   KIAA1217   KIF5B   KIN   KLF6   LARP4B   LRRC18   LYZL1   LYZL2   MAP3K8   MAPK8   MARCHF8   MASTL   MCM10   MEIG1   MINDY3   MIR1915   MIR1915HG   MKX   MLLT10   MPP7   MSRB2   MTPAP   MTRNR2L7   MYO3A   NEBL   NET1   NMT2   NPY4R   NRP1   NSUN6   NUDT5   ODAD2   OGDHL   OLAH   OPTN   OR13A1   OTUD1   PARD3   PDSS1   PFKFB3   PFKP   PGBD3   PHYH   PIP4K2A   PITRM1   PLXDC2   PRINS   PRKCQ   PROSER2   PRPF18   PRTFDC1   PTCHD3   PTER   PTF1A   PTPN20   RAB18   RASGEF1A   RASSF4   RBM17   RBP3   RET   RPP38   RPP38-DT   RSU1   SEC61A2   SEPHS1   SFMBT2   SKIDA1   SLC18A3   SLC39A12   SPAG6   ST8SIA6   STAM   SUV39H2   SVIL   SYT15   TAF3   TASOR2   THNSL1   TMEM273   TMEM72   TRDMT1   TUBAL3   UCMA   UCN3   UPF2   USP6NL   VIM   VSTM4   WAC   WASHC2C   WDFY4   WDR37   YME1L1   ZEB1   ZFAND4   ZMYND11   ZNF22   ZNF22-AS1   ZNF239   ZNF248   ZNF25   ZNF32   ZNF33A   ZNF33B   ZNF37A   ZNF438   ZNF485   ZNF488  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3710100,026 - 50,961,640CLINVAR
Cytogenetic Map1010p15.3-q11.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13443870
Created: 2017-11-07
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.