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Variant : CV672886 (GRCh37/hg19 2q37.3(chr2:241582582-242285265)x3) Homo sapiens

Symbol: CV672886
Name: GRCh37/hg19 2q37.3(chr2:241582582-242285265)x3
Condition: not provided [RCV000846002]
Clinical Significance: uncertain significance
Last Evaluated: 05/30/2018
Review Status: no assertion criteria provided
Related Genes: AGXT   ANO7   AQP12A   AQP12B   HDLBP   KIF1A   MAB21L4   MTERF4   PASK   PPP1R7   SEPTIN2   SNED1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372241,582,582 - 242,285,265CLINVAR
Cytogenetic Map22q37.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14976520
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-02-11
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.