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Variant : CV158060 (GRCh38/hg38 10p15.3-13(chr10:70478-15373336)x3) Homo sapiens

Symbol: CV158060
Name: GRCh38/hg38 10p15.3-13(chr10:70478-15373336)x3
Condition: See cases [RCV000137384]
Clinical Significance: uncertain significance
Last Evaluated: 10/10/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ACBD7   ADARB2   ADARB2-AS1   AKR1C1   AKR1C2   AKR1C3   AKR1C4   AKR1E2   ANKRD16   ASB13   ATP5F1C   BEND7   CALML3   CALML3-AS1   CALML5   CAMK1D   CCDC3   CDC123   CDNF   CELF2   CELF2-AS1   CELF2-AS2   DCLRE1C   DHTKD1   DIP2C   DIP2C-AS1   ECHDC3   FAM107B   FAM171A1   FBH1   FRMD4A   GATA3   GATA3-AS1   GDI2   GTPBP4   HSPA14   IDI1   IDI2   IDI2-AS1   IL15RA   IL2RA   ITIH2   ITIH5   KIN   KLF6   LARP4B   LINC00200   LINC00700   LINC00701   LINC00702   LINC00703   LINC00705   LINC00706   LINC00707   LINC00708   LINC00709   LINC00710   MANCR   MCM10   MEIG1   MIR1265   MIR3155A   MIR3155B   MIR4293   MIR4480   MIR4481   MIR548AK   MIR548Q   MIR5699   MIR6072   MIR6078   NET1   NMT2   NUDT5   OLAH   OPTN   PFKFB3   PFKP   PHYH   PITRM1   PITRM1-AS1   PRKCQ   PRKCQ-AS1   PROSER2   PROSER2-AS1   PRPF18   RBM17   RPP38   RPP38-DT   SEC61A2   SEPHS1   SFMBT2   SUV39H2   TAF3   TASOR2   TRV-TAC3-1   TUBAL3   TUBB8   UCMA   UCN3   UPF2   USP6NL   WDR37   ZMYND11  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_70478)_(15373336_?)dup
Human AssemblyChrPosition (strand)Source
GRCh381070,478 - 15,373,336CLINVAR
GRCh3710224,406 - 15,415,335 (+)CLINVAR
Build 3610106,418 - 15,455,341CLINVAR
Cytogenetic Map1010p15.3-13CLINVAR

Additional Information

CRRD Object Information
CRRD ID: 9484941
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2016-05-31
Status: ACTIVE


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