[1] are when a DNA segment of one kilobase or larger is pres…

[1] are when a DNA segment of one kilobase or larger is present at a variable copy number in comparison to the reference genome, and encompass [2] nucleotides per genome than SNPs and are [3] likely to cause health problems than SNPs. Common CNV’s in humans are [4] such as Huntington’s disease and spinocerebellar ataxia. Huntington’s disease is caused by a trinucleotide repeat [5] the coding sequence of the gene, while Fragile X syndrome is caused by a trinucleotide-repeat in the [6] region of the gene. The proposed mechanism for trinucleotide-repeat diseases is [7] which is thought to happen more often in regions of repeat during the process of [8].

In 2008, researchers discovered a genetic mutation in a man…

In 2008, researchers discovered a genetic mutation in a man that took place 6,000-10,000 years ago. He that is thought to be the first person to have the mutation that resulted in blue eyes, and would therefore be the source of all blue-eyed humans alive on the planet today. 

The recent announcement of the CRISPR-gene edited babies has…

The recent announcement of the CRISPR-gene edited babies has prompted many prominent scientists and bioethicists to propose strict new guidelines that restrict human germline editing to be restricted to serious genetic diseases, and recommends couples should first attempt IVF with pre-implantation genetic diagnosis.