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Variant : CV595266 (GRCh37/hg19 2q13(chr2:111392259-113217630)x1) Homo sapiens

Symbol: CV595266
Name: GRCh37/hg19 2q13(chr2:111392259-113217630)x1
Condition: not provided [RCV000740566]
Clinical Significance: uncertain significance
Last Evaluated: 01/03/2011
Review Status: no assertion criteria provided
Related Genes: ACOXL   ANAPC1   BCL2L11   BUB1   FBLN7   MERTK   RGPD8   TMEM87B   ZC3H6   ZC3H8  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372111,392,259 - 113,217,630CLINVAR
Cytogenetic Map22q13CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14355940
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-06-23
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.