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Variant : CV625962 (GRCh37/hg19 11q24.3(chr11:129060826-129712175)x3) Homo sapiens

Symbol: CV625962
Name: GRCh37/hg19 11q24.3(chr11:129060826-129712175)x3
Condition: See cases [RCV000790609]
Clinical Significance: uncertain significance
Last Evaluated: 09/28/2018
Review Status: criteria provided, single submitter
Related Genes: ARHGAP32   BARX2   TMEM45B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3711129,060,826 - 129,712,175CLINVAR
Cytogenetic Map1111q24.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14697864
Created: 2019-08-06
Species: Homo sapiens
Last Modified: 2020-07-28
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.