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Variant : CV383858 (GRCh37/hg19 6q21(chr6:109564793-112223595)x1) Homo sapiens

Symbol: CV383858
Name: GRCh37/hg19 6q21(chr6:109564793-112223595)x1
Condition: See cases [RCV000447293]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: AK9   AMD1   CD164   CDC40   CDK19   DDO   FIG4   FYN   GPR6   GTF3C6   METTL24   MFSD4B   MICAL1   PPIL6   REV3L   RPF2   SLC16A10   SLC22A16   SMPD2   TRAF3IP2   TRAF3IP2-AS1   WASF1   ZBTB24  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh376109,564,793 - 112,223,595CLINVAR
Cytogenetic Map66q21CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12852010
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-02-20
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.