tor2a[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
nsv6314154	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,306,022-130,522,616 , GRCh38.p12 chr9: 127,543,743-127,760,337	TOR2A, STXBP1, 6 more genes
nsv4350379	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,335,766-130,517,907 , GRCh38.p12 chr9: 127,573,487-127,755,628	TOR2A, STXBP1, 6 more genes
nsv6314148	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,392,953-130,526,044 , GRCh38.p12 chr9: 127,630,674-127,763,765	TOR2A, STXBP1, 5 more genes
nsv3899776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 129,370,440-133,866,894 , GRCh38.p12 chr9: 126,608,161-130,991,507	TOR2A, FNBP1, 136 more genes
nsv3917587	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 127,795,683-131,484,475 , GRCh38 chr9: 125,993,583-129,682,375 , GRCh37 chr9: 128,755,862-132,444,654	TOR2A, DYNC2I2, 115 more genes
nsv3924370	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 126,857,965-130,440,046 , GRCh38 chr9: 125,055,865-128,637,946 , GRCh37 chr9: 127,818,144-131,400,225	TOR2A, MVB12B, 97 more genes
nsv3903209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,390,139-132,760,275 , GRCh38.p12 chr9: 127,627,860-129,997,996	TOR2A, PTRH1, 99 more genes
nsv4768372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 128,512,347-130,702,572 , GRCh38.p12 chr9: 125,750,068-127,940,293	TOR2A, LOC105379841, 47 more genes
nsv3897949	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 129,079,208-130,851,795 , GRCh38.p12 chr9: 126,316,929-128,089,516	TOR2A, EEIG1, 44 more genes
nsv3921944	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 126,081,595-127,781,685 , NCBI36 chr9: 127,883,695-129,583,785 , GRCh37 chr9: 128,843,874-130,543,964	TOR2A, LOC101929116, 30 more genes
nsv5564479	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr9: 129,376,729-131,016,993 , GRCh38.p12 chr9: 126,614,450-128,254,714	TOR2A, PIP5KL1, 50 more genes
nsv4768374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,412,438-131,423,964 , GRCh38.p12 chr9: 127,650,159-128,661,685	TOR2A, COQ4, 53 more genes
nsv4450425	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr9: 130,374,663-131,329,276 , GRCh38 chr9: 127,612,384-128,566,997	TOR2A, RNU7-171P, 50 more genes
nsv6312681	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,216,807-130,953,136 , GRCh38.p12 chr9: 127,454,528-128,190,857	TOR2A, EEIG1, 32 more genes
nsv3912247	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981	TOR2A, ALOX15P2, 2184 more genes
nsv3890420	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,122,247 , GRCh38.p12 chr9: 10,590-138,231,797	TOR2A, TBC1D13, 2183 more genes
nsv3905118	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,114,095 , GRCh38.p12 chr9: 10,590-138,223,645	TOR2A, MIR219A2, 2183 more genes
nsv3891842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,107,672 , GRCh38.p12 chr9: 10,590-138,217,222	TOR2A, OR13C1P, 2183 more genes
nsv3895453	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 46,587-141,066,491 , GRCh38.p12 chr9: 46,587-138,172,039	TOR2A, RPL19P15, 2176 more genes
nsv3900967	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 163,131-141,122,114 , GRCh38.p12 chr9: 163,131-138,231,664	TOR2A, BANCR, 2173 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 44

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Number of Variants: 20

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