map2k7[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 9

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Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7095726	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 6,361,586-8,212,364 , GRCh38.p12 chr19: 6,361,575-8,147,480	MAP2K7, SLC25A23, 77 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	MAP2K7, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	MAP2K7, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	MAP2K7, LENG8, 2408 more genes
nsv3914351	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555	MAP2K7, SEMA6B, 299 more genes
nsv3890584	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 3,120,160-9,732,820 , GRCh38.p12 chr19: 3,120,162-9,622,144	MAP2K7, PCP2, 250 more genes
nsv7095676	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 7,586,521-8,670,595 , GRCh38.p12 chr19: 7,521,635-8,605,710	MAP2K7, LRRC8E, 53 more genes
nsv4676269	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 7,657,490-8,569,762 , GRCh38.p12 chr19: 7,592,604-8,504,878	MAP2K7, LRRC8E, 47 more genes
nsv4682037	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 7,587,617-8,373,194 , GRCh38.p12 chr19: 7,522,731-8,308,310	MAP2K7, XAB2, 40 more genes

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map2k7[All Fields] AND 1[has_clinical] (10)
dbVar
Glioblastoma stem-like cell lines, glioblastomas, and glioma cell lines
Glioblastoma stem-like cell lines, glioblastomas, and glioma cell lines
Accession: GDS3885

GEO DataSets
Related DataSets for GEO Profiles (Select 71359018) (1)
GEO DataSets

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