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

Variant : CV674072 (GRCh37/hg19 14q32.31-32.33(chr14:102931119-107285437)x1) Homo sapiens

Symbol: CV674072
Name: GRCh37/hg19 14q32.31-32.33(chr14:102931119-107285437)x1
Condition: not provided [RCV000847188]
Clinical Significance: pathogenic
Last Evaluated: 12/14/2017
Review Status: no assertion criteria provided
Related Genes: ADSS1   AHNAK2   AKT1   AMN   ANKRD9   ASPG   ATP5MPL   BAG5   BRF1   BTBD6   C14orf180   CDC42BPB   CDCA4   CEP170B   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   MTA1   NUDT14   PACS2   PLD4   PPP1R13B   RCOR1   RD3L   SIVA1   TDRD9   TECPR2   TEDC1   TEX22   TMEM121   TMEM179   TNFAIP2   TRAF3   TRMT61A   XRCC3   ZBTB42   ZFYVE21  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh3714102,931,119 - 107,285,437CLINVAR
Cytogenetic Map1414q32.31-32.33CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 14975320
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-07-28
Status: ACTIVE


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