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Variant : CV382557 (GRCh37/hg19 7q11.23(chr7:76946280-77011847)x3) Homo sapiens

Symbol: CV382557
Name: GRCh37/hg19 7q11.23(chr7:76946280-77011847)x3
Condition: See cases [RCV000449405]
Clinical Significance: likely benign
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: GSAP  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37776,946,280 - 77,011,847CLINVAR
Cytogenetic Map77q11.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12854101
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.