Analyzing Chromosome Mutations and Karyotypes

Analyzing Chromosome Mutations and Karyotypes

Assessment

Interactive Video

Biology

6th - 10th Grade

Easy

Created by

Olivia Brooks

Used 2+ times

FREE Resource

The video tutorial by Travis Spiver and his son Jordan Spiffy covers the four types of chromosome mutations: deletions, translocations, inversions, and duplications. It explains how these mutations can be analyzed using karyotypes and discusses the causes and effects of non-disjunction, which can lead to conditions like Down Syndrome and Turner Syndrome. The video also highlights the importance of understanding chromosome mutations for identifying genetic disorders. Viewers are encouraged to take a quiz to test their understanding of the material.

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10 questions

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1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the main focus of today's video?

Chromosome mutations

Cell division

Gene mutations

Protein synthesis

2.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

How many pairs of chromosomes do humans have in a normal karyotype?

24

22

23

46

3.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is non-disjunction?

The failure of paired chromosomes to separate during cell division

The process of chromosomes pairing up and exchanging genetic material

The duplication of genetic material on a chromosome

The deletion of a segment of a chromosome

4.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the cause of Down syndrome?

Deletion of a chromosome

Presence of an extra copy of chromosome 21

Inversion of a chromosome segment

Duplication of a chromosome

5.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which syndrome is caused by the deletion of parts or all of the chromosomes on the 23rd pair?

Turner syndrome

Down syndrome

Klinefelter syndrome

Hemophilia

6.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is a translocation mutation?

A chromosome segment is inverted

A chromosome segment breaks off and reattaches to another chromosome

A chromosome segment is duplicated

A chromosome segment is deleted

7.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

Which condition is characterized by moderate to severe intellectual disability and is caused by duplication of genetic material on the X chromosome?

Hemophilia

MECP2 duplication syndrome

Turner syndrome

Down syndrome

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