ocln[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
nsv5673655	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 69,509,142-69,514,109 , GRCh37 chr5: 68,804,969-68,809,936	OCLN
nsv3919694	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr5: 68,859,964-68,938,597 , GRCh38 chr5: 69,528,381-69,607,014 , GRCh37 chr5: 68,824,208-68,902,841	OCLN, RNU6-724P, 2 more genes
nsv4457177	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 68,753,608-68,831,651 , GRCh38.p12 chr5: 69,457,781-69,535,824 , GRCh38.p12 chr5\|NW_003315917.2: 240,721-318,768	OCLN, RPS27P14, 3 more genes
nsv3889956	copy number variation	1	nstd102	human	not provided	GRCh37 chr5: 68,757,774-68,828,296 , GRCh38 chr5: 69,461,947-69,532,469	OCLN, RPS27P14, 3 more genes
esv3648253	copy number variation	1	estd216	human	not provided	GRCh37 chr5: 68,757,774-68,828,296 , GRCh38.p12 chr5: 69,461,947-69,532,469 , GRCh38.p12 chr5\|NW_003315917.2: 244,886-315,409	OCLN, RPS27P14, 3 more genes
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	OCLN, MEGF10, 2080 more genes
nsv6313676	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 64,049,692-70,306,646 , GRCh38.p12 chr5: 64,753,865-71,010,819	OCLN, BCL9P1, 105 more genes
nsv3921568	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 64,228,590-68,791,331 , NCBI36 chr5: 64,264,346-68,827,087 , GRCh38 chr5: 64,932,763-69,495,504	OCLN, LOC100419549, 67 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	OCLN, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	OCLN, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	OCLN, SPEF2, 2490 more genes
nsv3911585	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550	OCLN, LINC02241, 878 more genes
nsv4578696	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr5: 58,780,641-73,523,380 , GRCh37.p13 chr5: 58,076,468-72,819,205	OCLN, TRIM23, 215 more genes
nsv3883692	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr5: 58,966,132-68,847,066 , GRCh38.p12 chr5: 59,670,306-69,551,239	OCLN, TRIM23, 125 more genes
nsv3920421	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr5: 62,538,695-70,622,774 , GRCh37 chr5: 62,502,939-70,587,018 , GRCh38 chr5: 63,207,112-71,291,191	OCLN, TRIM23, 124 more genes
nsv3915524	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 68,720,419-68,875,627 , GRCh38 chr5: 69,424,592-69,579,800	OCLN, MARVELD2, 6 more genes
nsv3888628	copy number variation	1	nstd102	human	Benign	GRCh37 chr5: 68,818,173-70,657,747 , GRCh38 chr5: 69,522,346-71,361,920	OCLN, LOC643367, 47 more genes
nsv3911382	copy number variation	1	nstd102	human	Benign	NCBI36 chr5: 68,859,795-70,693,465 , GRCh37.p13 chr5: 68,824,039-70,657,709 , GRCh38.p12 chr5: 69,528,212-71,361,882	OCLN, LOC728526, 47 more genes
nsv3911454	copy number variation	2	nstd102	human	Benign	NCBI36 chr5: 68,885,419-70,693,465 , GRCh37.p13 chr5: 68,849,663-70,657,709 , GRCh38.p12 chr5: 69,553,836-71,361,882	OCLN, GUSBP14, 45 more genes
nsv3910438	copy number variation	1	nstd102	human	Benign	GRCh38 chr5: 69,553,776-71,317,498 , NCBI36 chr5: 68,885,359-70,649,081 , GRCh37 chr5: 68,849,603-70,613,325	OCLN, LOC107986372, 43 more genes

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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 46

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Number of Variants: 20

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Supplemental Content

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