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Variant : CV595263 (GRCh37/hg19 2q13(chr2:110985804-111300000)x1) Homo sapiens

Symbol: CV595263
Name: GRCh37/hg19 2q13(chr2:110985804-111300000)x1
Condition: not provided [RCV000740563]
Clinical Significance: benign
Last Evaluated: 06/01/2011
Review Status: no assertion criteria provided
Related Genes: LIMS4   RGPD6  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372110,985,804 - 111,300,000CLINVAR
Cytogenetic Map22q13CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14355937
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-03-24
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.