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Variant : CV436963 (GRCh37/hg19 14q32.32-32.33(chr14:103965059-107285437)x1) Homo sapiens

Symbol: CV436963
Name: GRCh37/hg19 14q32.32-32.33(chr14:103965059-107285437)x1
Condition: See cases [RCV000511801]
Clinical Significance: pathogenic
Last Evaluated: 02/29/2016
Review Status: no assertion criteria provided
Related Genes: ADSS1   AHNAK2   AKT1   ASPG   ATP5MPL   BAG5   BRF1   BTBD6   C14orf180   CDCA4   CEP170B   CKB   CLBA1   COA8   CRIP1   CRIP2   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   RD3L   SIVA1   TDRD9   TEDC1   TEX22   TMEM121   TMEM179   TRMT61A   XRCC3   ZBTB42   ZFYVE21  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3714103,965,059 - 107,285,437CLINVAR
Cytogenetic Map1414q32.32-32.33CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13444770
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2019-11-12
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.