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Variant : CV675588 (GRCh37/hg19 14q32.12-32.33(chr14:91969028-107285437)x3) Homo sapiens

Symbol: CV675588
Name: GRCh37/hg19 14q32.12-32.33(chr14:91969028-107285437)x3
Condition: not provided [RCV000848687]
Clinical Significance: pathogenic
Last Evaluated: 10/04/2017
Review Status: no assertion criteria provided
Related Genes: ADSS1   AHNAK2   AK7   AKT1   AMN   ANKRD9   ASB2   ASPG   ATG2B   ATP5MPL   ATXN3   BAG5   BCL11B   BDKRB1   BDKRB2   BEGAIN   BRF1   BTBD6   BTBD7   C14orf132   C14orf177   C14orf180   CATSPERB   CCDC85C   CCNK   CDC42BPB   CDCA4   CEP170B   CHGA   CINP   CKB   CLBA1   CLMN   COA8   COX8C   CPSF2   CRIP1   CRIP2   CYP46A1   DDX24   DEGS2   DICER1   DIO3   DIO3OS   DLK1   DYNC1H1   EIF5   EML1   EVL   EXOC3L4   FAM181A   FBLN5   GLRX5   GOLGA5   GON7   GPR132   GSC   GSKIP   HHIPL1   HSP90AA1   IFI27   IFI27L1   IFI27L2   IGH   IGHA1   IGHA2   IGHD   IGHD3-3   IGHE   IGHG1   IGHG2   IGHG3   IGHG4   IGHM   IGHV3-23   INF2   ITPK1   JAG2   KIF26A   KLC1   LGMN   MARK3   MEG3   MEG8   MIR127   MIR134   MIR136   MIR203A   MIR369   MIR370   MIR376A1   MIR376A2   MIR376B   MIR376C   MIR380   MIR409   MIR410   MIR431   MIR433   MIR487B   MIR495   MOAP1   MOK   MTA1   NDUFB1   NUDT14   OTUB2   PACS2   PAPOLA   PLD4   PPP1R13B   PPP2R5C   PPP4R3A   PPP4R4   PRIMA1   RCOR1   RD3L   RIN3   RTL1   SERPINA1   SERPINA10   SERPINA11   SERPINA12   SERPINA2   SERPINA3   SERPINA4   SERPINA5   SERPINA6   SERPINA9   SETD3   SIVA1   SLC24A4   SLC25A29   SLC25A47   SNHG10   SNORD112   SNORD113-1   SNORD114-1   SYNE3   TC2N   TCL1A   TCL1B   TCL6   TDRD9   TECPR2   TEDC1   TEX22   TMEM121   TMEM179   TMEM251   TNFAIP2   TRAF3   TRIP11   TRMT61A   UBR7   UNC79   VRK1   WARS1   WDR20   WDR25   XRCC3   YY1   ZBTB42   ZFYVE21   ZNF839  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371491,969,028 - 107,285,437CLINVAR
Cytogenetic Map1414q32.12-32.33CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14975329
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2019-12-03
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.