21686 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv10221	copy number variation	7	nstd4	human		GRCh38.p12 chr2: 227,715,193-228,041,264 , NCBI35 chr2: 228,405,414-228,731,485 , GRCh37.p13 chr2: 228,579,909-228,905,980	CCL20, CRIPTOP2, 7 more genes

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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