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Variant : CV675788 (GRCh37/hg19 14q21.2(chr14:45563086-45643146)x1) Homo sapiens

Symbol: CV675788
Name: GRCh37/hg19 14q21.2(chr14:45563086-45643146)x1
Condition: not provided [RCV000848887]
Clinical Significance: uncertain significance
Last Evaluated: 01/12/2018
Review Status: no assertion criteria provided
Related Genes: FANCM   FKBP3   PRPF39  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371445,563,086 - 45,643,146CLINVAR
Cytogenetic Map1414q21.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14980419
Created: 2019-10-08
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.