Discover the comprehensive 'Associated Conditions' tab, where all conditions linked to genes within CNV variants are showcased. This tab provides valuable insights into the corresponding phenotypes entered into the case, allowing for a comprehensive understanding of the genetic associations and their related clinical manifestations

When you click on the 'Associated Conditions' tab, you will find tiles that provide an overview of conditions associated with your variant. These tiles offer indications of the relevance of the phenotypes you have indicated, evidence levels, inheritance models, and condition sources. If a condition consists of multiple sub-conditions, simply click on the tile to access more detailed information, including links to external sources.

Clicking on the condition will direct you to the dedicated condition page, providing access to additional information such as the condition's description, synonyms, associated phenotypes, and literature evidence. This comprehensive page offers a deeper understanding of the condition and facilitates further exploration