3669429 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv517354	copy number variation	9	nstd21	human		NCBI35 chr1: 109,494,079-109,538,178 , GRCh37.p13 chr1: 109,782,037-109,826,136 , GRCh38.p12 chr1: 109,239,415-109,283,514	CELSR2, PSRC1

dbGaP
Link from dbVar to dbGaP
Gene
Link from dbVar to Gene
GEO DataSets
Link from dbVar to GEO DataSets
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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