13q12.12 copy number variation (Homo sapiens)

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It is a risk variation for neuropsychiatric diseases like schizophrenia (Kirov et al. 2014, 10.1016/j.biopsych.2013.07.022) and with the presence of SACS it harbors a gene known for causing Spastic ataxia (MIM # 270550). </Comment> <Graphics BoardWidth="1170.0172860847001" BoardHeight="654.5"/> <DataNode TextLabel="LINC00362" Type="GeneProduct"> <Graphics CenterX="145.0" CenterY="190.9498703543648" Width="80.0" Height="20.0" ZOrder="32768" FontSize="12" Valign="Middle" Color="990099"/> <Xref Database="Ensembl" ID="ENSG00000229483"/> </DataNode> <DataNode TextLabel="LINC00327" Type="GeneProduct"> <Graphics CenterX="420.0" CenterY="190.9498703543648" Width="80.0" Height="20.0" ZOrder="32768" FontSize="12" Valign="Middle" Color="990099"/> <Xref Database="Ensembl" ID="ENSG00000232977"/> </DataNode> <DataNode TextLabel="LINC00352" Type="GeneProduct"> <Graphics CenterX="508.0" CenterY="190.9498703543648" Width="80.0" Height="20.0" ZOrder="32768" FontSize="12" Valign="Middle" Color="990099"/> 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