1002583 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv469378	copy number variation	1	nstd27	human		NCBI35 chr12: 50,689,377-50,727,817 , GRCh37.p13 chr12: 52,403,110-52,441,550 , GRCh38.p12 chr12: 52,009,326-52,047,766	TAMALIN, NR4A1, 1 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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