17696106 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv1037689	copy number variation	1	nstd100	human		NCBI36 chr11: 99,400,588-100,129,809 , GRCh37.p13 chr11: 99,895,378-100,624,599 , GRCh38.p12 chr11: 100,024,646-100,753,868	PPIAP43, CNTN5, 5 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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