Skip Navigation
Genetics Home Reference: your guide to understanding genetic conditions About   Site Map   Contact Us
 
Home A service of the U.S. National Library of Medicine®
0-9 | A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q-R | S | T | U | V | W | X | Y-Z

Inversion

Definition(s)

A chromosomal rearrangement in which a segment of genetic material is broken away from the chromosome, inverted from end to end, and re-inserted into the chromosome at the same breakage site. Balanced inversions (no net loss or gain of genetic material) are usually not associated with phenotypic abnormalities, although in some cases gene disruptions at the breakpoints can cause adverse phenotypic effects, including some known genetic diseases; unbalanced inversions (loss or gain of chromosome material) nearly always yield an abnormal phenotype.

Definition from: GeneReviewsThis link leads to a site outside Genetics Home Reference. from the University of Washington and the National Center for Biotechnology Information

Related discussion in the Handbook

See also Understanding Medical Terminology.

 
Published: December 16, 2014