48477078 - dbVar

Warning: The NCBI web site requires JavaScript to function. more...

Result Filters

loading data ...

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3913723	insertion	1	nstd102	human	Pathogenic	GRCh37 chr1: 209,803,256-209,803,256 , GRCh38 chr1: 209,629,911-209,629,911	LAMB3

Filters: Manage Filters

ClinVar
Clinical reports for this variation
Gene
Link from dbVar to Gene
OMIM
Link from dbVar to OMIM
Pathways + GO
Pathways, annotations and biological systems (BioSystems) that cite genes containing current variations.
PubMed
Link from dbVar to PubMed
Taxonomy
Link from dbVar to Taxonomy

Your browsing activity is empty.

Activity recording is turned off.

You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)