17685542 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv1027125	copy number variation	1	nstd100	human		NCBI36 chr8: 58,053,833-58,258,438 , GRCh37.p13 chr8: 57,891,279-58,095,884 , GRCh38.p12 chr8: 56,978,720-57,183,325 , GRCh38.p12 chr8\|NW_017852931.1: 1-156,998	BPNT2, LOC112268372, 1 more genes

Supplemental Content

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