6-Nitro-1-tetralone - 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
nsv4681940	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 64,776,231-65,336,138 , GRCh38.p12 chr6: 64,066,338-64,626,245	EYS
nsv5674225	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 162,206,900-162,622,150 , GRCh38.p12 chr6: 161,785,868-162,201,118	PRKN
nsv5673683	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 64,940,485-65,336,138 , GRCh38.p12 chr6: 64,230,592-64,626,245	EYS
nsv3922487	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 124,437,486-124,820,793 , GRCh38 chr6: 124,116,341-124,499,647 , NCBI36 chr6: 124,479,185-124,862,492	NKAIN2
nsv7097583	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 66,094,259-66,417,118 , GRCh38.p12 chr6: 65,384,366-65,707,225	EYS
nsv3910578	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 72,611,926-72,864,616 , GRCh38 chr6: 71,845,502-72,098,192 , GRCh37 chr6: 72,555,205-72,807,895	RIMS1
nsv6312584	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 65,098,563-65,336,158 , GRCh38.p12 chr6: 64,388,670-64,626,265	EYS
nsv5673780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 80,816,391-81,053,541 , GRCh38.p12 chr6: 80,106,674-80,343,824	BCKDHB
nsv7097594	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 80,816,411-81,053,521 , GRCh38.p12 chr6: 80,106,694-80,343,804	BCKDHB
nsv6290274	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 162,394,334-162,622,284 , GRCh38.p12 chr6: 161,973,302-162,201,252	PRKN
nsv7097449	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 66,200,477-66,417,039 , GRCh38.p12 chr6: 65,490,584-65,707,146	EYS
nsv4456916	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 107,573,260-107,767,076 , GRCh38.p12 chr6: 107,252,056-107,445,872	PDSS2
nsv7097071	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 65,146,047-65,336,158 , GRCh38.p12 chr6: 64,436,154-64,626,265	EYS
nsv3881428	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr6: 161,785,752-161,973,437 , GRCh37 chr6: 162,206,784-162,394,469	PRKN
nsv5674017	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 65,149,045-65,336,148 , GRCh38.p12 chr6: 64,439,152-64,626,255	EYS
nsv7097095	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 80,880,989-81,055,997 , GRCh38.p12 chr6: 80,171,272-80,346,280	BCKDHB
nsv7097338	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 51,586,774-51,752,053 , GRCh38.p12 chr6: 51,721,976-51,887,255	PKHD1
nsv6314670	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 64,776,385-64,940,484 , GRCh38.p12 chr6: 64,066,492-64,230,591	EYS
nsv3877972	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 64,066,492-64,230,591 , GRCh37.p13 chr6: 64,776,385-64,940,484	EYS
nsv6312394	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 64,791,739-64,940,727 , GRCh38.p12 chr6: 64,081,846-64,230,834	EYS

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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 81052

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Number of Variants: 20

Page of 4053

Supplemental Content

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