orc4[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
nsv6311219	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 148,693,079-148,716,455 , GRCh38.p12 chr2: 147,935,510-147,958,886	ORC4
nsv3889238	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 148,777,298-148,779,627 , GRCh38.p12 chr2: 148,019,729-148,022,058	ORC4, MBD5
nsv3889139	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 148,659,466-148,698,781 , GRCh38.p12 chr2: 147,901,897-147,941,212	ORC4, ACVR2A
nsv6313894	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 148,746,282-149,079,105 , GRCh38.p12 chr2: 147,988,713-148,321,536	ORC4, LOC105373673, 3 more genes
nsv4674335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 148,646,132-148,959,158 , GRCh38.p12 chr2: 147,888,563-148,201,589	ORC4, ACVR2A, 3 more genes
nsv4685947	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 148,710,290-149,021,799 , GRCh38.p12 chr2: 147,952,721-148,264,230	ORC4, LOC105373674, 2 more genes
nsv1398026	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 148,432,391-148,737,275 , GRCh37 chr2: 148,715,921-149,020,805 , GRCh38 chr2: 147,958,352-148,263,236	ORC4, LOC105373673, 2 more genes
nsv3881830	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 148,755,020-149,050,963 , GRCh38.p12 chr2: 147,997,451-148,293,394	ORC4, LOC105373673, 1 more genes
nsv6315419	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 148,698,834-148,954,778 , GRCh38.p12 chr2: 147,941,265-148,197,209	ORC4, LOC105373673, 2 more genes
nsv4728385	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 148,679,076-148,894,267 , GRCh38.p12 chr2: 147,921,507-148,136,698	ORC4, ACVR2A, 3 more genes
nsv3884725	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 148,777,552-148,991,171 , GRCh38.p12 chr2: 148,019,983-148,233,602	ORC4, LOC105373673, 1 more genes
nsv3906146	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 148,460,350-148,672,190 , GRCh37 chr2: 148,743,880-148,955,720 , GRCh38 chr2: 147,986,311-148,198,151	ORC4, LOC105373673, 2 more genes
nsv3888767	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 148,483,962-148,694,158 , GRCh38.p12 chr2: 147,726,393-147,936,589	ORC4, ACVR2A, 2 more genes
nsv6313630	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 148,698,523-148,900,148 , GRCh38.p12 chr2: 147,940,954-148,142,579	ORC4, LOC105373673, 2 more genes
nsv6291352	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 148,762,386-148,932,571 , GRCh38.p12 chr2: 148,004,817-148,175,002	ORC4, LOC105373673, 1 more genes
nsv4728164	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 148,746,282-148,897,425 , GRCh38.p12 chr2: 147,988,713-148,139,856	ORC4, MBD5, 2 more genes
nsv3876575	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 148,724,265-148,861,205 , GRCh38.p12 chr2: 147,966,696-148,103,636	ORC4, MBD5, 2 more genes
nsv3887205	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 148,728,326-148,851,964 , GRCh38.p12 chr2: 147,970,757-148,094,395	ORC4, MBD5, 2 more genes
nsv4674490	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 148,755,020-148,862,543 , GRCh38.p12 chr2: 147,997,451-148,104,974	ORC4, LOC105373673, 1 more genes
nsv6290235	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 148,726,315-148,824,342 , GRCh38.p12 chr2: 147,968,746-148,066,773	ORC4, MBD5, 2 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 73

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Number of Variants: 20

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