comt[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
nsv4457497	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr22: 19,932,833-19,945,742 , GRCh38.p12 chr22: 19,945,310-19,958,219	COMT
nsv3878411	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr22: 19,918,533-19,929,346 , GRCh38 chr22: 19,931,010-19,941,823	COMT, TXNRD2
nsv4457393	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr22: 19,905,801-19,938,011 , GRCh38.p12 chr22: 19,918,278-19,950,488	COMT, TXNRD2
nsv6311119	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr22: 19,929,214-19,929,336 , GRCh38.p12 chr22: 19,941,691-19,941,813	COMT, TXNRD2
nsv4681469	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr22: 19,864,618-19,929,336 , GRCh38.p12 chr22: 19,877,095-19,941,813	COMT, TXNRD2, 1 more genes
nsv6311315	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr22: 19,918,553-19,969,614 , GRCh38.p12 chr22: 19,931,030-19,982,091	COMT, ARVCF, 2 more genes
nsv6311176	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr22: 19,862,041-19,930,515 , GRCh38.p12 chr22: 19,874,518-19,942,992	COMT, RPL8P5, 1 more genes
nsv4451067	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr22: 19,864,618-19,929,336 , GRCh38 chr22: 19,877,095-19,941,813	COMT, TXNRD2, 1 more genes
nsv4674327	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,475,385-23,764,120 , GRCh38.p12 chr22: 17,992,619-23,421,933	COMT, GP1BB, 308 more genes
nsv3917936	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 18,659,766-22,152,986 , GRCh38 chr22: 18,339,130-23,480,799 , GRCh37 chr22: 20,279,766-23,822,986	COMT, IGLV7-46, 298 more genes
nsv4676119	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,899-20,730,144 , GRCh38.p12 chr22: 16,408,173-20,375,854	COMT, C22orf39, 150 more genes
nsv3923978	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 15,399,015-19,048,227 , GRCh37 chr22: 17,019,015-20,718,227 , GRCh38 chr22: 16,538,125-20,363,937	COMT, MIR185, 146 more genes
nsv4676296	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,899-20,125,005 , GRCh38.p12 chr22: 16,408,173-20,137,482	COMT, FAM230J, 139 more genes
nsv3895935	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,900-20,026,751 , GRCh38.p12 chr22: 16,408,174-20,039,228	COMT, FAM247C, 131 more genes
nsv3913197	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr22: 17,397,498-20,708,934 , GRCh38 chr22: 16,916,608-20,354,644 , NCBI36 chr22: 15,777,498-19,038,934	COMT, E2F6P1, 128 more genes
nsv3910919	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr22: 15,777,498-18,691,763 , GRCh37 chr22: 17,397,498-20,311,763 , GRCh38 chr22: 16,916,608-20,324,240	COMT, C22orf39, 127 more genes
nsv3901351	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,644,790-21,915,509 , GRCh38.p12 chr22: 18,162,023-21,561,220	COMT, RPL34P35, 149 more genes
nsv6634411	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,639,780-21,910,280 , GRCh38.p12 chr22: 18,157,013-21,555,991	COMT, RIMBP3C, 149 more genes
nsv3912933	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 17,008,132-20,213,879 , GRCh37.p13 chr22: 18,628,132-21,883,879 , GRCh38.p12 chr22: 18,145,365-21,529,590	COMT, KLHL22, 146 more genes
nsv3907554	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,626,108-21,800,797 , GRCh38.p12 chr22: 18,143,341-21,446,508	COMT, RNY1P9, 144 more genes

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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 337

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Number of Variants: 20

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