53150523 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6112678	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 16,370,960-16,383,841 , GRCh38.p12 chr1: 16,044,465-16,057,346	FAM131C, CLCNKB

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ClinVar
Clinical reports for this variation
Gene
Link from dbVar to Gene
OMIM
Link from dbVar to OMIM
Pathways + GO
Pathways, annotations and biological systems (BioSystems) that cite genes containing current variations.
Taxonomy
Link from dbVar to Taxonomy

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