Deletion: a segment of the chromosome is lost during breakage. Duplication: a segment of the chromosome is copied and inserted back into the chromosome following breakage. Inversion: a segment of the chromosome is reversed and re-inserted following breakage. Translocation: a segment of the chromosome breaks off and joins a different chromosome.
A chromosome inversion is a type of structural change in a chromosome where a segment of DNA is reversed in orientation. This can lead to disruptions in gene expression and potential issues during cell division. Inversions can be balanced or unbalanced, depending on whether there is a loss or gain of genetic material.
Inversion is the process that changes the order of genes on a chromosome without altering the number of genes. It involves a segment of the chromosome being flipped in orientation. This can result in changes in gene expression and potentially lead to genetic disorders.
When a segment of a chromosome is turned 180 degrees, it is called an inversion. Inversions can have different effects depending on the location of the inversion and the genes involved. They can disrupt gene expression and potentially lead to genetic disorders or infertility, or they can have no noticeable effect on the individual.
The type of mutation that results in the reversal of the direction of part of the chromosome is called an inversion mutation. It occurs when a segment of the chromosome breaks and is reinserted in the opposite orientation. This can disrupt the normal functioning of genes located within the inverted region.
An Inversion mutation is a mutation that causes a reversal in the order of a segment of a chromosome within the chromosome, or a gene.
An inversion in meteorology is when atmospheric pressure causes an abnormal condition. An example would be that the pressure causes warmer air to sink closer to earth's surface and cooler air to rise higher. When this inversion happens, one of the effects is that pollution and smog stay trapped within our atmosphere.
Deletion: Part of a chromosome is missing. Duplication: A segment of a chromosome is copied multiple times. Inversion: A segment of a chromosome is reversed in orientation. Translocation: Part of a chromosome breaks off and attaches to another chromosome.
Inversion occurs when a fragment of a chromosome is reversed
Deletion: a segment of the chromosome is lost during breakage. Duplication: a segment of the chromosome is copied and inserted back into the chromosome following breakage. Inversion: a segment of the chromosome is reversed and re-inserted following breakage. Translocation: a segment of the chromosome breaks off and joins a different chromosome.
I'm pretty sure that the answer is an INVERSION
A chromosome inversion is a type of structural change in a chromosome where a segment of DNA is reversed in orientation. This can lead to disruptions in gene expression and potential issues during cell division. Inversions can be balanced or unbalanced, depending on whether there is a loss or gain of genetic material.
Inversion.
The four types of chromosomal mutation are deletion, duplication, inversion and trasnlocation. Deletion is the loss of all or part of a chromosome. Duplication is where a segment of a chromosome is copied. Inversion is where a section of a chromosome is reversed. Translocation is the process in where a part of one chromosome breaks off and attaches to a non-homologous chromosome.
Inversion is the process that changes the order of genes on a chromosome without altering the number of genes. It involves a segment of the chromosome being flipped in orientation. This can result in changes in gene expression and potentially lead to genetic disorders.
A chromosome that has been broken and rejoined in a reversal sequence has undergone an inversion mutation. This can lead to changes in gene expression and potentially affect the phenotype of an organism.
When a segment of a chromosome is turned 180 degrees, it is called an inversion. Inversions can have different effects depending on the location of the inversion and the genes involved. They can disrupt gene expression and potentially lead to genetic disorders or infertility, or they can have no noticeable effect on the individual.