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Variant : CV676721 (GRCh37/hg19 22q12.3(chr22:36704833-36911784)x3) Homo sapiens

Symbol: CV676721
Name: GRCh37/hg19 22q12.3(chr22:36704833-36911784)x3
Condition: not provided [RCV000849820]
Clinical Significance: uncertain significance
Last Evaluated: 02/14/2018
Review Status: no assertion criteria provided
Related Genes: EIF3D   FOXRED2   MYH9   TXN2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372236,704,833 - 36,911,784CLINVAR
Cytogenetic Map2222q12.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14981315
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-01-14
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.