In mammalian females, most genes on one X chromosome are transcriptionally silenced as a result of X chromosome inactivation, Whereas it is well established that some X-linked genes "escape'' X inactivation and are expressed from both active (Xa) and inactive (Xi) X chromosomes, most models for the chromosomal control of X-linked gene expression assume that the X inactivation status of a given gene is constant among different females within a population. In this report, we test the expression of human S-linked genes in primary cell lines from females with complete nonrandom X inactivation by using transcribed polymorphisms to distinguish Sa and Si expression, Six X-linked genes used to document this assay system show ed monoallelic expression in all informative cell lines, consistent with X inactivation, However, a novel pattern of expression was observed for another gene, REP1; monoallelic expression, indicating inactivation, was detected in some lines, whereas biallelic expression, indicating escape from inactivation, H-as detected in others. Furthermore, levels of Si expression,varied among cell lines that expressed REP1, The cellular basis of Si expression uas examined by expression assays in single cells. These data indicate that REP1 is expressed from the Xi in all cells, but that the level of expression relative to Sa levels is reduced. These findings suggest that Si gene expression is under a previously unsuspected level of genetic or epigenetic control, likely involving local or regional changes in chromatin organization that determine whether a gene escapes or is subject to X inactivation.