prkcg[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3885084	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 53,906,892-53,906,993 , GRCh37 chr19: 54,410,146-54,410,247	PRKCG
nsv5564521	insertion	1	nstd102	human	Uncertain significance	GRCh38 chr19: 53,880,584-53,880,584 , GRCh37 chr19: 54,383,838-54,383,838	PRKCG
nsv4683322	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 54,376,784-54,396,645 , GRCh38.p12 chr19: 53,873,530-53,893,391	PRKCG, MYADM
nsv5381201	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 54,297,303-54,410,149 , GRCh38.p12 chr19: 53,794,049-53,906,895	PRKCG, MYADM-AS1, 2 more genes
nsv3890020	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 54,280,799-54,635,178 , GRCh38.p12 chr19: 53,777,545-54,071,460	PRKCG, MIR373, 12 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	PRKCG, 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	PRKCG, 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	PRKCG, LENG8, 2408 more genes
nsv3919076	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 48,432,832-59,083,573 , NCBI36 chr19: 53,124,644-63,775,385 , GRCh38 chr19: 47,929,575-58,572,206	PRKCG, KCNA7, 697 more genes
nsv3911950	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 48,411,797-59,051,332 , NCBI36 chr19: 53,103,609-63,743,144 , GRCh38 chr19: 47,908,540-58,539,965	PRKCG, LOC107987270, 694 more genes
nsv3924732	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 49,907,832-58,557,889 , GRCh37 chr19: 50,411,089-59,069,256 , NCBI36 chr19: 55,102,901-63,761,068	PRKCG, RPL39P37, 556 more genes
nsv4729755	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886	PRKCG, SIGLEC5, 574 more genes
nsv3890862	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 50,489,390-59,095,359 , GRCh38.p12 chr19: 49,986,133-58,583,992	PRKCG, SIGLECL1, 552 more genes
nsv3923909	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 55,347,589-63,784,382 , GRCh37 chr19: 50,655,777-59,092,570 , GRCh38 chr19: 50,152,520-58,581,203	PRKCG, OSCAR, 535 more genes
nsv3891963	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 50,740,074-59,097,160 , GRCh38.p12 chr19: 50,236,817-58,585,793	PRKCG, RPS9, 535 more genes
nsv3916611	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 50,694,476-59,047,185 , NCBI36 chr19: 55,386,288-63,738,997 , GRCh38 chr19: 50,191,219-58,535,818	PRKCG, RNU6-980P, 526 more genes
nsv3922599	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 51,141,518-58,539,965 , NCBI36 chr19: 56,336,587-63,743,144 , GRCh37 chr19: 51,644,775-59,051,332	PRKCG, LOC100421130, 475 more genes
nsv3913991	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 57,338,938-63,648,700 , GRCh37 chr19: 52,647,126-58,956,888 , GRCh38 chr19: 52,143,873-58,445,521	PRKCG, PEG3, 398 more genes
nsv3923613	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 52,612,432-58,581,203 , GRCh37 chr19: 53,115,685-59,092,570 , NCBI36 chr19: 57,807,497-63,784,382	PRKCG, ZNF71-SMIM17, 393 more genes
nsv3919766	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 58,150,121-63,784,382 , GRCh37 chr19: 53,458,309-59,092,570 , GRCh38 chr19: 52,955,056-58,581,203	PRKCG, MIR520F, 382 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 30

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Number of Variants: 20

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Supplemental Content

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