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Variant : CV605926 (GRCh37/hg19 15q13.2(chr15:30354303-31089526)x3) Homo sapiens

Symbol: CV605926
Name: GRCh37/hg19 15q13.2(chr15:30354303-31089526)x3
Condition: not provided [RCV000751226]
Clinical Significance: benign
Last Evaluated: 01/26/2017
Review Status: no assertion criteria provided
Related Genes: ARHGAP11B   CHRFAM7A   GOLGA8H   GOLGA8J  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371530,354,303 - 31,089,526CLINVAR
Cytogenetic Map1515q13.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14366552
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-10-15
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.