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Variant : CV601514 (GRCh37/hg19 7q11.23(chr7:74772735-74837045)x0) Homo sapiens

Symbol: CV601514
Name: GRCh37/hg19 7q11.23(chr7:74772735-74837045)x0
Condition: not provided [RCV000746814]
Clinical Significance: benign
Last Evaluated: 09/20/2012
Review Status: no assertion criteria provided
Related Genes: CASTOR2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37774,772,735 - 74,837,045CLINVAR
Cytogenetic Map77q11.23CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14362161
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-01-07
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.