mapk10[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
nsv3889725	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 86,976,413-87,010,825 , GRCh38.p12 chr4: 86,055,260-86,089,672	MAPK10
nsv3879013	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 87,007,954-87,028,072 , GRCh38.p12 chr4: 86,086,801-86,106,919	MAPK10
nsv3886930	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 87,007,954-87,027,857 , GRCh38.p12 chr4: 86,086,801-86,106,704	MAPK10
nsv3887604	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 87,014,729-87,028,072 , GRCh38.p12 chr4: 86,093,576-86,106,919	MAPK10
nsv3881982	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr4: 87,156,443-87,275,696 , GRCh38.p12 chr4: 86,235,290-86,354,543	MAPK10, RN7SKP96
nsv3884011	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 87,039,732-87,104,170 , GRCh38.p12 chr4: 86,118,579-86,183,017	MAPK10, MAPK10-AS1
nsv3883932	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 87,119,830-87,159,318 , GRCh38.p12 chr4: 86,198,677-86,238,165	MAPK10, MAPK10-AS1
nsv3889913	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 87,118,930-87,156,742 , GRCh38.p12 chr4: 86,197,777-86,235,589	MAPK10, MAPK10-AS1
nsv3888060	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 87,119,830-87,156,742 , GRCh38.p12 chr4: 86,198,677-86,235,589	MAPK10, MAPK10-AS1
nsv3886384	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 87,119,830-87,153,443 , GRCh38.p12 chr4: 86,198,677-86,232,290	MAPK10, MAPK10-AS1
nsv3875980	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 87,118,081-87,142,271 , GRCh38.p12 chr4: 86,196,928-86,221,118	MAPK10, MAPK10-AS1
nsv3872065	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 87,119,830-87,142,271 , GRCh38.p12 chr4: 86,198,677-86,221,118	MAPK10, MAPK10-AS1
nsv3878046	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 87,119,830-87,141,521 , GRCh38.p12 chr4: 86,198,677-86,220,368	MAPK10, MAPK10-AS1
nsv3884646	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 87,119,830-87,141,384 , GRCh38.p12 chr4: 86,198,677-86,220,231	MAPK10, MAPK10-AS1
nsv3875439	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 87,119,830-87,141,106 , GRCh38.p12 chr4: 86,198,677-86,219,953	MAPK10, MAPK10-AS1
nsv3884114	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 87,119,830-87,139,772 , GRCh38.p12 chr4: 86,198,677-86,218,619	MAPK10, MAPK10-AS1
nsv4457334	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 87,306,927-87,496,888 , GRCh38.p12 chr4: 86,385,774-86,575,735	MAPK10, MIR4452
nsv4455931	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 86,911,035-86,983,232 , GRCh38.p12 chr4: 85,989,882-86,062,079	MAPK10, ARHGAP24
nsv4457185	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 86,913,748-86,983,232 , GRCh38.p12 chr4: 85,992,595-86,062,079	MAPK10, ARHGAP24
nsv3913791	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 86,923,241-86,972,445 , NCBI36 chr4: 87,142,265-87,191,469 , GRCh38 chr4: 86,002,088-86,051,292	MAPK10, ARHGAP24

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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 54

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Number of Variants: 20

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Supplemental Content

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