{"pos":200,"chromosome":"chr1","length":1254,"type":"duplication","end":1454,"publication_counts":null,"regions":{},"coding_gene_id":[],"coding_genes":null,"exon":null,"gene_symbol":null,"gene_id":null,"genes":[],"transcripts":[],"camouflaged_regions":[],"sv_acmg_annotation":{"verdict":{"saphetor_class":"Benign","saphetor_score":-1.0,"verdict":"Uncertain Significance","approx_score":-0.6},"classifications":[{"saphetor_score":-1.0,"approx_score":0.0,"acmg_class":"Uncertain Significance","saphetor_class":"Benign","name":"Gene","saphetor_user_explain":{"Benign":["This structural variant affects 0 coding genes."]}},{"saphetor_score":0.0,"approx_score":-0.6,"acmg_class":"Uncertain Significance","saphetor_class":"Uncertain Significance","name":"Content","user_explain":{"Uncertain Significance":["This structural variant doesn't affect any known domain or coding genes."]}},{"saphetor_score":0.0,"approx_score":0.0,"acmg_class":"Uncertain Significance","saphetor_class":"Uncertain Significance","name":"Inheritance"},{"saphetor_score":0.0,"approx_score":0.0,"acmg_class":"Uncertain Significance","saphetor_class":"Uncertain Significance","name":"Literature"},{"saphetor_score":0.0,"approx_score":0.0,"acmg_class":"Uncertain Significance","saphetor_class":"Uncertain Significance","name":"Overlap"}],"sample_findings":{"mode_of_inheritance":"Assumed AD/AR."},"version_name":"12.5.1"},"deleted_data_reason":null,"publications":{"regions":[],"genes":[]},"cytobands":"1p36.33"}