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Variant : CV435969 (GRCh37/hg19 14q32.33(chr14:105814886-107285437)x1) Homo sapiens

Symbol: CV435969
Name: GRCh37/hg19 14q32.33(chr14:105814886-107285437)x1
Condition: See cases [RCV000511369]
Clinical Significance: uncertain significance
Last Evaluated: 02/05/2015
Review Status: no assertion criteria provided
Related Genes: CRIP1   CRIP2   IGH   IGHA1   IGHA2   IGHD   IGHD3-3   IGHE   IGHG1   IGHG2   IGHG3   IGHG4   IGHM   IGHV3-23   MTA1   PACS2   TEDC1   TEX22   TMEM121  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3714105,814,886 - 107,285,437CLINVAR
Cytogenetic Map1414q32.33CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13444341
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-02-11
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.