30349670 - dbVar - NCBI

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Number of Variants: 1

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv1398678	copy number variation	1285	nstd116	human		GRCh37 chr8: 7,286,416-7,366,833 , GRCh37 chr8: 7,669,242-7,740,180 , GRCh38.p12 chr8: 7,428,894-7,509,311 , GRCh38.p12 chr8: 7,811,720-7,882,658 , GRCh38.p12 chr8\|NW_018654717.1: 710,045-790,472 , GRCh38.p12 chr8\|NW_018654717.1: 5,408,965-5,479,946 , GRCh38.p12 chr8\|NT_187570.1: 111,965-192,414	SPAG11B, DEFB103B, 10 more genes

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Related information

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

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"nstd116"[study] AND "copy number variation"[variant_type] (2)
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