11894314 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv930479	copy number variation	1	nstd78	human		GRCh37 chr12: 104,659,052-104,659,669 , GRCh38.p12 chr12: 104,265,274-104,265,891	TXNRD1, RPL18AP3

Functional Class
Functional class of the sequence domain architecture
Gene
Link from dbVar to Gene
Nucleotide
Link from dbVar to Nucleotide
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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