coq10b[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
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	COQ10B, DAZAP2P1, 2991 more genes
nsv3894939	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 175,471,822-204,514,516 , GRCh37 chr2: 175,763,576-204,806,271 , GRCh38 chr2: 174,898,848-203,941,548	COQ10B, TRE-TTC9-1, 412 more genes
nsv6315398	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 185,697,659-213,002,074 , GRCh38.p12 chr2: 184,832,932-212,137,349	COQ10B, LOC107985785, 381 more genes
nsv3899404	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 176,877,419-202,612,758 , GRCh37 chr2: 177,169,173-202,904,513 , GRCh38 chr2: 176,304,445-202,039,790	COQ10B, LINC01877, 326 more genes
nsv3896612	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 192,938,826-215,705,052 , NCBI36 chr2: 193,511,797-216,278,020 , GRCh37 chr2: 193,803,552-216,569,775	COQ10B, MTND4P30, 320 more genes
nsv3895293	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 178,738,797-199,390,216 , NCBI36 chr2: 178,447,043-199,098,461 , GRCh38 chr2: 177,874,070-198,525,492	COQ10B, CALCRL-AS1, 218 more genes
nsv6637127	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 189,909,904-209,468,383 , GRCh38.p12 chr2: 189,045,178-208,603,658	COQ10B, LOC100421409, 310 more genes
nsv3891560	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 186,027,472-201,059,372 , NCBI36 chr2: 186,600,444-201,632,340 , GRCh37 chr2: 186,892,199-201,924,095	COQ10B, AOX1, 174 more genes
nsv6636571	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 187,152,754-199,960,525 , GRCh38.p12 chr2: 186,288,027-199,095,802	COQ10B, GAPDHP59, 135 more genes
nsv3884561	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 189,490,490-200,615,496 , GRCh38.p12 chr2: 188,625,763-199,750,773	COQ10B, C2orf88, 120 more genes
nsv3884912	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 191,750,202-202,297,376 , GRCh38.p12 chr2: 190,885,476-201,432,653	COQ10B, CLK1, 134 more genes
nsv4716529	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 190,345,272-200,212,289 , GRCh38.p12 chr2: 189,480,546-199,347,566	COQ10B, C2orf66, 105 more genes
nsv3881119	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 193,537,927-202,027,736 , GRCh38.p12 chr2: 192,673,201-201,163,013	COQ10B, LOC105376755, 107 more genes
nsv3908231	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 196,233,563-204,542,456 , GRCh38 chr2: 195,660,594-203,969,488 , GRCh37 chr2: 196,525,318-204,834,211	COQ10B, LINC01877, 170 more genes
nsv3876959	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 194,581,315-201,752,422 , GRCh38.p12 chr2: 193,716,591-200,887,699	COQ10B, LOC101927741, 87 more genes
nsv4453090	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 195,786,723-200,531,127 , GRCh38.p12 chr2: 194,921,999-199,666,404	COQ10B, RFTN2, 54 more genes
nsv3875157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 196,581,377-200,947,041 , GRCh38.p12 chr2: 195,716,653-200,082,318	COQ10B, C2orf66, 53 more genes
nsv3907002	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 195,379,883-199,410,661 , GRCh38 chr2: 194,515,159-198,545,937 , NCBI36 chr2: 195,088,128-199,118,906	COQ10B, LOC105373817, 47 more genes
nsv4768322	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 197,359,024-201,383,462 , GRCh38.p12 chr2: 196,494,300-200,518,739	COQ10B, ANKRD44-DT, 48 more genes
nsv6313482	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 197,586,481-200,793,870 , GRCh38.p12 chr2: 196,721,757-199,929,147	COQ10B, RPL4P7, 38 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 42

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Number of Variants: 20

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Supplemental Content

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Search details

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