{"type":"video","version":"1.0","html":"<iframe src=\"https://www.loom.com/embed/864448bbd23c45c9b995c3e538cc8aa3\" frameborder=\"0\" width=\"1920\" height=\"1440\" webkitallowfullscreen mozallowfullscreen allowfullscreen></iframe>","height":1440,"width":1920,"provider_name":"Loom","provider_url":"https://www.loom.com","thumbnail_height":1440,"thumbnail_width":1920,"thumbnail_url":"https://cdn.loom.com/sessions/thumbnails/864448bbd23c45c9b995c3e538cc8aa3-0a5bfcaf43de901c.gif","duration":557.835,"title":"TrackGene Genome Variant Monitoring Overview","description":"This Loom demonstrates the current state of Genome Variant Monitoring within TrackGene. It shows how a test for Mary Melbourne with breast cancer consent is manually entered using a dummy Exemplar Genomics report, recording an overall positive BRCA1 result with two variants, one likely pathogenic and one likely benign, reviewed on the day entered. Entering the variants automatically creates a genotype record and highlights discrepancies between the local laboratory interpretation and ClinVar, including conflicting classifications that should be monitored. It also notes plans to use FHIR for automated results intake and mentions notifications on the TrackGene home screen for follow up activities like case reviews. "}