Better look for create manual variant from search result

In variant search, we collect/combine Search Results with a create manual variant, using the variant identifier

This will probably fail on super large indels, and also you lose the information of how you got there, ie it might have gotten there via searching for "GATA2:c.1110dup"

Gives you a bunch of info:

```
Variant via HGVS Search "GATA2:c.1110dup"
Results for: ENST00000341105.7 (MANE), NM_032638.5 (MANE)
Warning: GATA2 has 8 other transcripts in GRCh37 that may resolve to different coordinates. You may wish to search for the gene symbol to view all results
Using transcript ENST00000341105 version 2 instead of provided version 7
ENST00000341105.7:c.1110dup resolved to genomic coordinates 3:128200694 T>TG
NM_032638.5:c.1110dup resolved to genomic coordinates 3:128200694 T>TG
3:128200694 T>TG Click to create and annotate this variant
```

But the only thing it actually stores on create manual variant is "3:128200694 T>TG"

You could store lots, and show to people how you got there (ie show search, and results/suggestions)

Still need to group by variant ID but maybe launch from one of NM_032638.5:c.1110dup/ENST00000341105.7:c.1110dup