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Variant : CV436214 (GRCh37/hg19 4q21.22-21.23(chr4:83954528-85807754)x1) Homo sapiens

Symbol: CV436214
Name: GRCh37/hg19 4q21.22-21.23(chr4:83954528-85807754)x1
Condition: See cases [RCV000510348]
Clinical Significance: uncertain significance
Last Evaluated: 06/23/2014
Review Status: no assertion criteria provided
Related Genes: ABRAXAS1   CDS1   COPS4   COQ2   GPAT3   HELQ   HPSE   MRPS18C   NKX6-1   PLAC8   WDFY3  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37483,954,528 - 85,807,754CLINVAR
Cytogenetic Map44q21.22-21.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13443327
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2019-12-03
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.