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Variant : CV555286 (GRCh37/hg19 14q11.2(chr14:23240787-23468899)x1) Homo sapiens

Symbol: CV555286
Name: GRCh37/hg19 14q11.2(chr14:23240787-23468899)x1
Condition: not provided [RCV000683591]
Clinical Significance: uncertain significance
Last Evaluated: 08/14/2017
Review Status: no assertion criteria provided
Related Genes: AJUBA   C14orf93   HAUS4   LRP10   MMP14   MRPL52   OXA1L   PRMT5   RBM23   REM2   SLC7A7  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371423,240,787 - 23,468,899CLINVAR
Cytogenetic Map1414q11.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13797129
Created: 2018-10-09
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.