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Variant : CV554402 (GRCh37/hg19 6q21(chr6:110419878-111698827)x1) Homo sapiens

Symbol: CV554402
Name: GRCh37/hg19 6q21(chr6:110419878-111698827)x1
Condition: not provided [RCV000682707]
Clinical Significance: uncertain significance
Last Evaluated: 12/21/2017
Review Status: no assertion criteria provided
Related Genes: AMD1   CDC40   CDK19   DDO   GTF3C6   METTL24   MFSD4B   REV3L   RPF2   SLC16A10   SLC22A16   WASF1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh376110,419,878 - 111,698,827CLINVAR
Cytogenetic Map66q21CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13795576
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.