stat1[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
nsv7096223	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 191,843,562-191,845,415 , GRCh38.p12 chr2: 190,978,836-190,980,689	STAT1
nsv4681251	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 191,835,409-191,835,463 , GRCh38.p12 chr2: 190,970,683-190,970,737	STAT1
nsv6636880	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 191,796,439-191,859,919 , GRCh38.p12 chr2: 190,931,713-190,995,193	STAT1, RAB1AP1, 1 more genes
nsv7096595	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr2: 191,835,429-192,012,929 , GRCh38.p12 chr2: 190,970,703-191,148,203	STAT1, STAT4, 4 more genes
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	STAT1, 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	STAT1, 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	STAT1, 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	STAT1, LINC01877, 326 more genes
nsv4451512	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 167,329,586-192,756,373 , GRCh38.p12 chr2: 166,473,076-191,891,647	STAT1, LINC01117, 339 more genes
nsv4674757	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 174,690,039-195,521,582 , GRCh38.p12 chr2: 173,825,311-194,656,858	STAT1, OSBPL6, 256 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	STAT1, 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	STAT1, LOC100421409, 310 more genes
nsv3878976	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 177,315,153-196,375,520 , GRCh38.p12 chr2: 176,450,425-195,510,796	STAT1, FSIP2-AS1, 202 more genes
nsv3900193	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 178,692,457-195,990,053 , NCBI36 chr2: 178,400,703-195,698,298 , GRCh38 chr2: 177,827,730-195,125,329	STAT1, OSBPL6, 171 more genes
nsv3905582	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 176,086,763-193,201,970 , NCBI36 chr2: 176,659,737-193,774,941 , GRCh37 chr2: 176,951,491-194,066,696	STAT1, RPL23AP35, 211 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	STAT1, 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	STAT1, 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	STAT1, 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	STAT1, CLK1, 134 more genes
nsv3898686	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 182,623,428-192,880,118 , GRCh38 chr2: 181,758,701-192,015,392 , NCBI36 chr2: 182,331,673-192,588,363	STAT1, KRT18P19, 111 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 41

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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