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

Variant : CV675318 (GRCh37/hg19 14q32.31-32.33(chr14:101627916-107147698)x1) Homo sapiens

Symbol: CV675318
Name: GRCh37/hg19 14q32.31-32.33(chr14:101627916-107147698)x1
Condition: not provided [RCV000848417]
Clinical Significance: pathogenic
Last Evaluated: 09/18/2017
Review Status: no assertion criteria provided
Related Genes: ADSS1   AHNAK2   AKT1   AMN   ANKRD9   ASPG   ATP5MPL   BAG5   BRF1   BTBD6   C14orf180   CDC42BPB   CDCA4   CEP170B   CINP   CKB   CLBA1   COA8   CRIP1   CRIP2   DIO3   DIO3OS   DYNC1H1   EIF5   EXOC3L4   GPR132   HSP90AA1   IGH   IGHA1   IGHA2   IGHD   IGHD3-3   IGHE   IGHG1   IGHG2   IGHG3   IGHG4   IGHM   IGHV3-23   INF2   JAG2   KIF26A   KLC1   MARK3   MIR203A   MOK   MTA1   NUDT14   PACS2   PLD4   PPP1R13B   PPP2R5C   RCOR1   RD3L   SIVA1   TDRD9   TECPR2   TEDC1   TEX22   TMEM121   TMEM179   TNFAIP2   TRAF3   TRMT61A   WDR20   XRCC3   ZBTB42   ZFYVE21   ZNF839  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3714101,627,916 - 107,147,698CLINVAR
Cytogenetic Map1414q32.31-32.33CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14975326
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2019-12-03
Status: ACTIVE



NHLBI Logo

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