48582789 - 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
nsv3971772	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 53,306,793-53,321,761 , GRCh37.p13 chr12: 53,700,577-53,715,545	AAAS, MYG1

Filters: Manage Filters

ClinVar
Clinical reports for this variation
Functional Class
Functional class of the sequence domain architecture
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.
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)