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Variant : CV248388 (GRCh37/hg19 11q25(chr11:134019210-134746628)x3) Homo sapiens

Symbol: CV248388
Name: GRCh37/hg19 11q25(chr11:134019210-134746628)x3
Condition: See cases [RCV000240041]
Clinical Significance: uncertain significance
Last Evaluated: 01/20/2016
Review Status: criteria provided, single submitter
Related Genes: ACAD8   B3GAT1   GLB1L2   GLB1L3   JAM3   LINC02714   NCAPD3   THYN1   VPS26B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3711134,019,210 - 134,746,628CLINVAR
Cytogenetic Map1111q25CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 11541506
Created: 2016-10-11
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.