1028768 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv470275	copy number variation	1	nstd30	human		NCBI36 chr12: 21,829,811-22,017,581 , GRCh38.p12 chr12: 21,785,610-21,973,380 , GRCh37.p13 chr12: 21,938,544-22,126,314	ABCC9, LOC105369689

dbSNP
Link from dbVar to dbSNP
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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