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Variant : CV437173 (GRCh37/hg19 15p13-q11.2(chr15:2770421-23082442)x1) Homo sapiens

Symbol: CV437173
Name: GRCh37/hg19 15p13-q11.2(chr15:2770421-23082442)x1
Condition: See cases [RCV000510203]
Clinical Significance: likely benign
Last Evaluated: 06/22/2015
Review Status: no assertion criteria provided
Related Genes: CYFIP1   GOLGA6L1   GOLGA6L6   NIPA1   NIPA2   OR4M2   OR4N4   POTEB   POTEB2   TUBGCP5  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37152,770,421 - 23,082,442CLINVAR
Cytogenetic Map1515p13-q11.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13443183
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2019-10-08
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.