17657095 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv998678	copy number variation	1	nstd100	human		NCBI36 chr1: 21,763,830-21,813,610 , GRCh37.p13 chr1: 21,891,243-21,941,023 , GRCh38.p12 chr1: 21,564,750-21,614,530	ALPL, RAP1GAP, 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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