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With increased use of chromosome microarray and exome sequencing, the frequency with which these CNVs are detected is increasing. While individuals with such CNVs often receive genetic counseling, research shows that associated psychiatric conditions are less often addressed\u2014clinicians tend to focus on the nonpsychiatric manifestations of the CNV. This represents an important service gap for people with these CNVs and their families, as research shows that not only do these families want genetic counseling about psychiatric illness, it can also produce meaningful positive outcomes for people, including increases in empowerment, and self\u2010efficacy. Therefore, there is a need to ensure that individuals with psychiatric condition\u2010associated CNVs are being counseled about these manifestations of their condition in a way that can promote the best outcomes. In this paper we describe the process of providing genetic counseling in two clinical scenarios in which a psychiatric susceptibility CNV is identified: (1) in an individual who has not been diagnosed with a psychiatric condition and (2) in an individual with an established psychiatric condition.<\/jats:p>","DOI":"10.1111\/cge.14210","type":"journal-article","created":{"date-parts":[[2022,8,22]],"date-time":"2022-08-22T23:43:07Z","timestamp":1661211787000},"page":"369-378","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":13,"title":["Psychiatric genetic counseling for people with copy number variants associated with psychiatric conditions"],"prefix":"10.1111","volume":"102","author":[{"given":"Emily","family":"Morris","sequence":"first","affiliation":[{"name":"Department of Medical Genetics University of British Columbia  Vancouver British Columbia Canada"},{"name":"Department of Psychiatry University of British Columbia  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