3679946 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv527871	copy number variation	1	nstd21	human		NCBI35 chr22: 36,799,196-36,805,159 , GRCh37.p13 chr22: 38,474,696-38,480,659 , GRCh38.p12 chr22: 38,078,689-38,084,652	SLC16A8, BAIAP2L2, 1 more genes

dbGaP
Link from dbVar to dbGaP
Functional Class
Functional class of the sequence domain architecture
Gene
Link from dbVar to Gene
GEO DataSets
Link from dbVar to GEO DataSets
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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