1028643 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv470150	copy number variation	1	nstd30	human		GRCh38.p12 chr19: 49,618,821-49,856,789 , GRCh37.p13 chr19: 50,122,078-50,360,046 , NCBI36 chr19: 54,813,890-55,051,858	AP2A1, PRMT1, 21 more genes

dbSNP
Link from dbVar to dbSNP
Functional Class
Functional class of the sequence domain architecture
Gene
Link from dbVar to Gene
GEO DataSets
Link from dbVar to GEO DataSets
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

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