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Variant : CV605847 (GRCh37/hg19 14q32.33(chr14:105781428-106016434)x1) Homo sapiens

Symbol: CV605847
Name: GRCh37/hg19 14q32.33(chr14:105781428-106016434)x1
Condition: not provided [RCV000751147]
Clinical Significance: benign
Last Evaluated: 12/06/2010
Review Status: no assertion criteria provided
Related Genes: BRF1   CRIP1   CRIP2   MTA1   PACS2   TEDC1   TEX22   TMEM121  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3714105,781,428 - 106,016,434CLINVAR
Cytogenetic Map1414q32.33CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14366473
Created: 2019-02-12
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.