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Variant : CV384140 (GRCh37/hg19 7q11.23(chr7:75058408-77082896)x1) Homo sapiens

Symbol: CV384140
Name: GRCh37/hg19 7q11.23(chr7:75058408-77082896)x1
Condition: See cases [RCV000449141]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: CCDC146   CCL24   CCL26   DTX2   FGL2   GSAP   HIP1   HSPB1   MDH2   POM121C   POMZP3   POR   RHBDD2   SPDYE5   SRRM3   SSC4D   STYXL1   TMEM120A   YWHAG   ZP3  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37775,058,408 - 77,082,896CLINVAR
Cytogenetic Map77q11.23CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12853838
Created: 2017-04-11
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.