50057678 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4578236	copy number variation	1	nstd180	human		GRCh37.p13 chrX\|NW_004070891.1: 575,570-575,650 , GRCh37.p13 chrX: 114,141,331-114,141,411 , GRCh38 chrX: 114,906,768-114,906,848	HTR2C

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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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