21535 - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv10070	copy number variation	12	nstd4	human		NCBI35 chr2: 87,963,455-88,100,866 , GRCh37.p13 chr2: 88,124,193-88,261,604 , GRCh38.p12 chr2: 87,824,674-87,962,085	RGPD2, MTATP8P2, 1 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

nsv10070 (1)
dbVar
Homo sapiens isolate CHM13 chromosome 10, alternate assembly T2T-CHM13v2.0
Homo sapiens isolate CHM13 chromosome 10, alternate assembly T2T-CHM13v2.0
gi|2194973501|gnl|ASM:GCF_009914825 ef|NC_060934.1||gpp|GPC_000012749.1||gnl|NCBI_GENOMES|119570

Nucleotide
BioAssay by Target (List) for Gene (Select 81603) (12)
PubChem BioAssay
PANX3 pannexin 3 [Homo sapiens]
PANX3 pannexin 3 [Homo sapiens]
Gene ID:116337

Gene
116337[uid] AND (alive[prop]) (1)
Gene

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