I think you mean translocation between chromosomes 13 and 14.
Transfiguration is a type of magic taught at Hogwarts School of Wizardry or, on a far more profound level, can also refer to the episode in the life of Christ where he appears before the disciples radiating light.
Well in eukaryotic cells each chromosome has a telomere on each end (to prevent it from unraveling), but I'm not 100% certain that these telomeres are identical although they contain very long repetitions of the same nucleotides. But in bacteria the chromosome is ring shaped and is all genes (there are no noncoding sequences, e.g. centromeres, telomeres, introns, pseudogenes, transposons) so there are no identical parts.
Deletions are a loss of all or part of a chromosome. Duplications produce extra copies of parts of a chromosome. Inversions reverse the direction of parts of a chromosome. Translocations occur when part of one chromosome breaks off and attaches to another.
Chromosomal deletion is a genetic mutation where a part of a chromosome is missing. This can lead to the loss of specific genes, which can cause genetic disorders and other health problems in individuals. Deletions can vary in size and can affect different parts of the chromosome.
The gene within a chromosome contains the specific sequence of nucleotides that codes for the amino acid sequence of a protein. This gene is transcribed into messenger RNA (mRNA), which is then translated into a specific sequence of amino acids during protein synthesis.
This answer will discuss the parts of a eukaryotic chromosome. Chromosomes consist of highly condensed DNA also called chromatin. The chromatin is organized into two arms: the shorter p arm and the longer q arm. Each chromosome contains a highly condensed region that separates the arms of the chromosome. This condensed region is called the centromere. The terminal ends of the chromosome are called telomere.
Children born without parts of chromosome 16 can have problems with growth disorders and anomalies with the head, face and internal organs.
Telomere - The ends of the chromosome. Centromere - The primary constriction of the chromosome. Chromatid - A single molecule of DNA. The centromere also divides the chromosome into a short arm (p) and a long arm (q).
The Centromere
Centromere.
The parts of a chromosome that control inherited traits is referred to as genes. There are many types of inherited traits, some visible while the others are invisible,
An exchange of chromosome segments is called a translocation. In genetics, it refers to a chromosome abnormality caused by rearrangement of parts between nonhomologous chromosomes.
chromatid
There is the xiphoid process (a small piece of cartilage at the base of your sternum)XX chromosome...orXY chromosome:)
Look at the nuts and bolts that hold the parts on. They will have tool marks on them if they have been removed.
pattern of sugar
Chromatids
The two genes are located on different chromosomes and therefore cannot be considered part of the same chromosome. Each chromosome consists of a single linear double-stranded DNA molecule and may contain numerous genes.