1260100 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv510756	copy number variation	2	nstd49	human		GRCh38.p12 chr19: 14,926,456-14,952,143 , GRCh37.p13 chr19: 15,037,268-15,062,955 , NCBI35 chr19: 14,898,268-14,923,955	SLC1A6, OR7A15P, 1 more genes

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