essv6842258 - dbVar - NCBI

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Number of Variants: 2

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
esv2743882	copy number variation	2	estd201	human		GRCh37 chr11: 994,865-995,167 , GRCh38.p12 chr11: 994,865-995,167 , GRCh38.p12 chr11\|NT_187681.1: 64,306-64,608 , GRCh38.p12 chr11\|NT_187656.1: 57,608-57,910	AP2A2
esv2743878	copy number variation	453	estd201	human		GRCh37 chr11: 864,732-1,510,882 , GRCh38.p12 chr11: 864,732-1,489,652	, MUC2, 18 more genes

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essv6842258 (2)
dbVar
essv5746420 (2)
dbVar
PMC Links for GEO Profiles (Select 122897365) (140)
PMC
PMC Links for GEO Profiles (Select 86173047) (301)
PMC
SLC14A1 solute carrier family 14 member 1 (Kidd blood group) [Homo sapiens]
SLC14A1 solute carrier family 14 member 1 (Kidd blood group) [Homo sapiens]
Gene ID:6563

Gene

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