osbpl6[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
nsv3906450	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 179,071,826-179,188,986 , GRCh38 chr2: 178,207,099-178,324,259	OSBPL6
nsv3881984	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 179,058,818-179,059,599 , GRCh38.p12 chr2: 178,194,091-178,194,872	OSBPL6
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	OSBPL6, 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	OSBPL6, TRE-TTC9-1, 412 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	OSBPL6, 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	OSBPL6, 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	OSBPL6, DNAJC19P5, 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	OSBPL6, CALCRL-AS1, 218 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	OSBPL6, FSIP2-AS1, 202 more genes
nsv4768307	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 163,078,055-182,119,617 , GRCh38.p12 chr2: 162,221,545-181,254,890	OSBPL6, RBM45, 258 more genes
nsv3904056	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 164,821,892-183,059,789 , NCBI36 chr2: 164,530,138-182,768,034 , GRCh38 chr2: 163,965,382-182,195,062	OSBPL6, PRKRA, 256 more genes
nsv3891673	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 172,285,743-190,044,294 , GRCh38 chr2: 171,429,233-189,179,568 , NCBI36 chr2: 171,993,989-189,752,539	OSBPL6, LOC729141, 238 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	OSBPL6, LOC105373771, 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	OSBPL6, RPL23AP35, 211 more genes
nsv3894385	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 170,972,444-186,762,866 , GRCh37 chr2: 171,264,198-187,054,621 , GRCh38 chr2: 170,407,688-186,189,894	OSBPL6, KRT18P29, 220 more genes
nsv3892770	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 175,499,230-189,865,690 , GRCh38 chr2: 174,634,502-189,000,964 , NCBI36 chr2: 175,207,476-189,573,935	OSBPL6, LOC401021, 179 more genes
nsv4454648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 173,538,954-186,401,606 , GRCh38.p12 chr2: 172,674,226-185,536,879	OSBPL6, PDE11A, 176 more genes
nsv5381341	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 171,999,572-182,774,361 , GRCh38.p12 chr2: 171,143,062-181,909,634	OSBPL6, ALDH7A1P2, 174 more genes
nsv3888432	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 174,238,257-181,604,341 , GRCh38.p12 chr2: 173,373,529-180,739,614	OSBPL6, LRRC2P1, 125 more genes
nsv3920257	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 173,710,846-180,977,641 , GRCh37.p13 chr2: 174,002,600-181,269,396 , GRCh38.p12 chr2: 173,137,872-180,404,669	OSBPL6, LINC01117, 128 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 38

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

Recent activity