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Variant : CV555038 (GRCh37/hg19 11q22.1(chr11:100507403-101123672)x3) Homo sapiens

Symbol: CV555038
Name: GRCh37/hg19 11q22.1(chr11:100507403-101123672)x3
Condition: not provided [RCV000683343]
Clinical Significance: likely benign
Last Evaluated: 01/19/2018
Review Status: no assertion criteria provided
Related Genes: ARHGAP42   PGR  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3711100,507,403 - 101,123,672CLINVAR
Cytogenetic Map1111q22.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13796595
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2019-12-03
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.