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Variant : CV435365 (GRCh37/hg19 14q32.31-32.33(chr14:102670706-107285437)x1) Homo sapiens

Symbol: CV435365
Name: GRCh37/hg19 14q32.31-32.33(chr14:102670706-107285437)x1
Condition: See cases [RCV000511173]
Clinical Significance: pathogenic
Last Evaluated: 08/01/2014
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   EIF5   EXOC3L4   GPR132   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   RCOR1   RD3L   SIVA1   TDRD9   TECPR2   TEDC1   TEX22   TMEM121   TMEM179   TNFAIP2   TRAF3   TRMT61A   WDR20   XRCC3   ZBTB42   ZFYVE21   ZNF839  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh3714102,670,706 - 107,285,437CLINVAR
Cytogenetic Map1414q32.31-32.33CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 13444148
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-08-04
Status: ACTIVE


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