17668143 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv1009726	copy number variation	1	nstd100	human		NCBI36 chr3: 139,702,613-140,220,378 , GRCh37.p13 chr3: 138,219,923-138,737,688 , GRCh38.p12 chr3: 138,501,081-139,018,846	FAIM, PRR23A, 11 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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