25018582 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv1127027	copy number variation	1	nstd106	human		GRCh37 chr22: 18,126,559-18,129,911 , GRCh38.p12 chr22: 17,643,793-17,647,145	BCL2L13

BioProjects
Link from dbVar to BioProjects
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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