17664358 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv1005941	copy number variation	1	nstd100	human		NCBI36 chr1: 167,677,110-167,723,017 , GRCh37.p13 chr1: 169,410,486-169,456,393 , GRCh38.p12 chr1: 169,441,248-169,487,155	CCDC181, SLC19A2

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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