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Variant : CV820725 (NC_000015.10:g.(?_63042820)_(63869153_?)dup) Homo sapiens

Symbol: CV820725
Name: NC_000015.10:g.(?_63042820)_(63869153_?)dup
Condition: Hypertrophic cardiomyopathy [RCV001033641]
Clinical Significance: uncertain significance
Last Evaluated: 11/03/2019
Review Status: criteria provided, single submitter
Related Genes: APH1B   CA12   FBXL22   HERC1   LACTB   RAB8B   RPS27L   TPM1   USP3  
Variant Type: duplication (SO:1000035)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_63042820)_(63869153_?)dup
NC_000015.9:g.(?_63335019)_(64161352_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh371563,335,019 - 64,161,352CLINVAR
Cytogenetic Map1515q22.2-22.31CLINVAR



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 26898654
Created: 2020-05-12
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.