22119 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv10654	copy number variation	88	nstd4	human		NCBI35 chr5: 729,285-1,135,688 , GRCh37.p13 chr5: 676,285-1,082,688 , GRCh38.p12 chr5: 676,170-1,082,573	TRIP13, SLC12A7, 10 more genes

Functional Class
Functional class of the sequence domain architecture
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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