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Variant : CV554639 (GRCh37/hg19 8p23.1(chr8:11679160-11888763)x3) Homo sapiens

Symbol: CV554639
Name: GRCh37/hg19 8p23.1(chr8:11679160-11888763)x3
Condition: not provided [RCV000682944]
Clinical Significance: likely benign
Last Evaluated: 02/27/2018
Review Status: no assertion criteria provided
Related Genes: CTSB   DEFB134   DEFB135   DEFB136   FDFT1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37811,679,160 - 11,888,763CLINVAR
Cytogenetic Map88p23.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13795845
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-06-30
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.