# Variant page top bar

<figure><img src="https://1131024994-files.gitbook.io/~/files/v0/b/gitbook-x-prod.appspot.com/o/spaces%2FGCW0DnLlE7QjoZPNmKIi%2Fuploads%2Fgit-blob-6abed9ac0807a7dc87546274b43006cdc3776229%2Fvariant%20page%20top%20bar%20new.png?alt=media" alt=""><figcaption></figcaption></figure>

## The variant page top bar displays, from left to right:

{% stepper %}
{% step %}
**Case ID**
{% endstep %}

{% step %}
**Gene symbol(s)**
{% endstep %}

{% step %}
**Variant type**
{% endstep %}

{% step %}
**Variant type-specific information:**

* **Small variant and mtDNA:** Genomic location and sequence change
* **CNV and SV:** Chromosome: start-end, length, and CNV/SV type
* **STR:** Chromosome: start–end, repeat unit, reference number of repeats and alternative number of repeats
* **Haplotype:** Chromosome: start–end and haplotype name
* **LOH/ROH:** Chromosome: start–end and length
  {% endstep %}

{% step %}
**Variant interpretation notes**
{% endstep %}

{% step %}
[**Variant tag**](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/variant_page/variant_tagging_widget)
{% endstep %}

{% step %}
[**Curate Variants export menu**](https://help.connected.illumina.com/emedgene/emedgene-curate-manual/curate_variants/how_to_add_a_variant_to_curate#id-2.-export-from-the-variant-page)
{% endstep %}
{% endstepper %}