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Variant : CV605715 (GRCh37/hg19 14q22.1(chr14:52890163-53288450)x1) Homo sapiens

Symbol: CV605715
Name: GRCh37/hg19 14q22.1(chr14:52890163-53288450)x1
Condition: not provided [RCV000751015]
Clinical Significance: benign
Last Evaluated: 10/19/2010
Review Status: no assertion criteria provided
Related Genes: ERO1A   GNPNAT1   GPR137C   PSMC6   STYX   TXNDC16  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh371452,890,163 - 53,288,450CLINVAR
Cytogenetic Map1414q22.1CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 14366341
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-02-11
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.