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Variant : CV554567 (GRCh37/hg19 7q11.23(chr7:75384846-76279036)x3) Homo sapiens

Symbol: CV554567
Name: GRCh37/hg19 7q11.23(chr7:75384846-76279036)x3
Condition: not provided [RCV000682872]
Clinical Significance: uncertain significance
Last Evaluated: 11/07/2017
Review Status: no assertion criteria provided
Related Genes: CCL24   CCL26   DTX2   HSPB1   MDH2   POMZP3   POR   RHBDD2   SRRM3   SSC4D   STYXL1   TMEM120A   YWHAG   ZP3  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37775,384,846 - 76,279,036CLINVAR
Cytogenetic Map77q11.23CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13795770
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-01-21
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.