Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV674134 (GRCh37/hg19 19q13.33(chr19:49600909-51366070)x3) Homo sapiens

Symbol: CV674134
Name: GRCh37/hg19 19q13.33(chr19:49600909-51366070)x3
Condition: not provided [RCV000847250]
Clinical Significance: uncertain significance
Last Evaluated: 05/12/2017
Review Status: no assertion criteria provided
Related Genes: ACP4   ADM5   AKT1S1   ALDH16A1   AP2A1   ASPDH   ATF5   BCL2L12   C19orf48   C19orf73   C19orf81   CD37   CLEC11A   CPT1C   DKKL1   EMC10   FAM71E1   FCGRT   FLT3LG   FUZ   GPR32   HRC   IL4I1   IRF3   IZUMO2   JOSD2   KASH5   KCNC3   KLK1   KLK15   KLK3   LIN7B   LRRC4B   MED25   MIR150   MYBPC2   MYH14   NAPSA   NOSIP   NR1H2   NUP62   PIH1D1   PNKP   POLD1   PPFIA3   PRMT1   PRR12   PRRG2   PTH2   PTOV1   PTOV1-AS2   RCN3   RPL13A   RPS11   RRAS   SCAF1   SHANK1   SIGLEC11   SLC17A7   SLC6A16   SNRNP70   SPIB   SYT3   TBC1D17   TEAD2   TRPM4   TSKS   VRK3   ZNF473  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371949,600,909 - 51,366,070CLINVAR
Cytogenetic Map1919q13.33CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14977828
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-06-23
Status: ACTIVE



NHLBI Logo

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