17676316 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv1017899	copy number variation	1	nstd100	human		NCBI36 chr8: 42,487,037-42,560,979 , GRCh37.p13 chr8: 42,367,880-42,441,822 , GRCh38.p12 chr8: 42,510,362-42,586,679	SMIM19, SLC20A2

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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