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Variant : CV436226 (GRCh37/hg19 17q25.2-25.3(chr17:75104943-75602123)x3) Homo sapiens

Symbol: CV436226
Name: GRCh37/hg19 17q25.2-25.3(chr17:75104943-75602123)x3
Condition: See cases [RCV000510636]
Clinical Significance: uncertain significance
Last Evaluated: 02/24/2015
Review Status: no assertion criteria provided
Related Genes: SEC14L1   SEPTIN9  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371775,104,943 - 75,602,123CLINVAR
Cytogenetic Map1717q25.2-25.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13443615
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-05-26
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.