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Variant : CV674983 (GRCh37/hg19 10p15.3-13(chr10:100026-15273144)x3) Homo sapiens

Symbol: CV674983
Name: GRCh37/hg19 10p15.3-13(chr10:100026-15273144)x3
Condition: not provided [RCV000848090]
Clinical Significance: pathogenic
Last Evaluated: 05/19/2017
Review Status: no assertion criteria provided
Related Genes: ACBD7   ADARB2   AKR1C1   AKR1C2   AKR1C3   AKR1C4   AKR1E2   ANKRD16   ASB13   ATP5F1C   BEND7   CALML3   CALML3-AS1   CALML5   CAMK1D   CCDC3   CDC123   CDNF   CELF2   DCLRE1C   DHTKD1   DIP2C   ECHDC3   FAM107B   FAM171A1   FBH1   FRMD4A   GATA3   GDI2   GTPBP4   HSPA14   IDI1   IDI2   IL15RA   IL2RA   ITIH2   ITIH5   KIN   KLF6   LARP4B   MCM10   MEIG1   NET1   NMT2   NUDT5   OLAH   OPTN   PFKFB3   PFKP   PHYH   PITRM1   PRKCQ   PROSER2   PRPF18   RBM17   RPP38   RPP38-DT   SEC61A2   SEPHS1   SFMBT2   SUV39H2   TAF3   TASOR2   TUBAL3   UCMA   UCN3   UPF2   USP6NL   WDR37   ZMYND11  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3710100,026 - 15,273,144CLINVAR
Cytogenetic Map1010p15.3-13CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14979655
Created: 2019-10-08
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.