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Variant : CV605752 (GRCh37/hg19 14q24.2(chr14:73373094-73702874)x3) Homo sapiens

Symbol: CV605752
Name: GRCh37/hg19 14q24.2(chr14:73373094-73702874)x3
Condition: not provided [RCV000751052]
Clinical Significance: likely benign
Last Evaluated: 09/27/2016
Review Status: no assertion criteria provided
Related Genes: DCAF4   PSEN1   RBM25   ZFYVE1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371473,373,094 - 73,702,874CLINVAR
Cytogenetic Map1414q24.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14366378
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.