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1q21.1 copy number variations and ANKRD35

Shortcuts: Differences, Similarities, Jaccard Similarity Coefficient, References.

Difference between 1q21.1 copy number variations and ANKRD35

1q21.1 copy number variations vs. ANKRD35

1q21.1 copy number variations (CNVs)Understanding the impact of 1q21.1 Copy Number Variant; C. Harvard et al; Orphanet Journal of Rare Diseases 2011, 6:54; are rare aberrations of human chromosome 1. Ankyrin repeat domain 35 also known as ANKRD35 is a protein which in humans is encoded by the ANKRD35 gene.

Similarities between 1q21.1 copy number variations and ANKRD35

1q21.1 copy number variations and ANKRD35 have 3 things in common (in Unionpedia): TAR syndrome, 1q21.1 deletion syndrome, 1q21.1 duplication syndrome.

TAR syndrome

TAR Syndrome (thrombocytopenia with absent radius) is a rare genetic disorder that is characterized by the absence of the radius bone in the forearm and a dramatically reduced platelet count.

1q21.1 copy number variations and TAR syndrome · ANKRD35 and TAR syndrome · See more »

1q21.1 deletion syndrome

1q21.1 deletion syndrome or 1q21.1 (recurrent) microdeletion is a rare aberration of chromosome 1.

1q21.1 copy number variations and 1q21.1 deletion syndrome · 1q21.1 deletion syndrome and ANKRD35 · See more »

1q21.1 duplication syndrome

1q21.1 duplication syndrome or 1q21.1 (recurrent) microduplication is a rare aberration of chromosome 1.

1q21.1 copy number variations and 1q21.1 duplication syndrome · 1q21.1 duplication syndrome and ANKRD35 · See more »

The list above answers the following questions

1q21.1 copy number variations and ANKRD35 Comparison

1q21.1 copy number variations has 38 relations, while ANKRD35 has 5. As they have in common 3, the Jaccard index is 6.98% = 3 / (38 + 5).

References

This article shows the relationship between 1q21.1 copy number variations and ANKRD35. To access each article from which the information was extracted, please visit:

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