orc5[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
nsv3908472	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 103,772,610-103,773,849 , GRCh38.p12 chr7: 104,132,163-104,133,402	ORC5
nsv3900182	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 103,813,499-103,870,718 , GRCh38.p12 chr7: 104,173,051-104,230,270	ORC5
nsv6636231	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 103,746,409-104,002,334 , GRCh38.p12 chr7: 104,105,962-104,361,886	ORC5, LHFPL3
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	ORC5, RNU6-438P, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	ORC5, LOC107986817, 2014 more genes
nsv3924380	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 101,912,320-120,918,695 , GRCh38 chr7: 102,196,924-121,278,641 , NCBI36 chr7: 101,626,924-120,705,931	ORC5, LOC102724434, 222 more genes
nsv6313576	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 100,676,872-119,156,160 , GRCh38.p12 chr7: 101,033,591-119,516,106	ORC5, LHFPL3-AS2, 233 more genes
nsv6313503	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 99,417,471-111,586,308 , GRCh38.p12 chr7: 99,819,848-111,946,253	ORC5, GJC3, 237 more genes
nsv3912378	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 101,807,149-112,414,850 , GRCh37 chr7: 101,450,429-112,054,905 , NCBI36 chr7: 101,237,149-111,842,141	ORC5, DNAJC2, 139 more genes
nsv3918078	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 102,235,882-105,128,791 , GRCh37 chr7: 102,448,646-105,341,555 , GRCh38 chr7: 102,808,199-105,701,108	ORC5, LHFPL3, 40 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	ORC5, RNU6-565P, 2684 more genes
nsv4455091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017	ORC5, RPL23AP51, 2684 more genes
nsv3909087	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620	ORC5, MNX1-AS2, 2682 more genes
nsv3908592	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017	ORC5, TRGV3, 2682 more genes
nsv3922815	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 96,887,100-158,409,214 , GRCh38 chr7: 97,419,852-158,923,762 , GRCh37 chr7: 97,049,164-158,716,453	ORC5, SEPTIN7P6, 1175 more genes
nsv3894097	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 98,693,388-159,119,707 , GRCh38.p12 chr7: 99,095,765-159,327,017	ORC5, CYP3A5, 1144 more genes
nsv3920103	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 100,955,796-104,860,145 , GRCh38 chr7: 101,525,795-105,432,462 , GRCh37 chr7: 101,169,076-105,072,909	ORC5, RNU6-1322P, 66 more genes
nsv6315223	complex substitution	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017	ORC5, AOC1, 2682 more genes
nsv4352523	inversion	1	nstd102	human	Pathogenic	GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550	ORC5, ACHE, 1532 more genes
nsv3904050	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr7: 102,910,570-105,104,800 , GRCh38.p12 chr7: 103,270,123-105,464,353	ORC5, RELN, 22 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 24

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Number of Variants: 20

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Supplemental Content

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