17717651 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv1059234	copy number variation	1	nstd100	human		NCBI36 chr22: 49,345,839-49,402,766 , GRCh37.p13 chr22: 50,998,973-51,055,900 , GRCh38.p12 chr22: 50,560,544-50,617,472	LOC107985568, SYCE3, 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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