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Variant : CV555309 (GRCh37/hg19 14q21.2(chr14:45548350-46158043)x3) Homo sapiens

Symbol: CV555309
Name: GRCh37/hg19 14q21.2(chr14:45548350-46158043)x3
Condition: not provided [RCV000683614]
Clinical Significance: likely benign
Last Evaluated: 07/10/2017
Review Status: no assertion criteria provided
Related Genes: FANCM   FKBP3   MIS18BP1   PRPF39  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371445,548,350 - 46,158,043CLINVAR
Cytogenetic Map1414q21.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13797183
Created: 2018-10-09
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.