17336790 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv997148	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 154,487,519-154,493,874 , GRCh38.p12 chrX: 155,258,234-155,264,589	RAB39B

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BioProjects
Link from dbVar to BioProjects
Functional Class
Functional class of the sequence domain architecture
Gene
Link from dbVar to Gene
OMIM
Link from dbVar to OMIM
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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