epdr1[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
nsv4456473	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 37,818,456-37,987,652 , GRCh38.p12 chr7: 37,778,854-37,948,050	EPDR1, NME8, 2 more genes
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	EPDR1, 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	EPDR1, LOC107986817, 2014 more genes
nsv3897424	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 32,911,003-44,576,005 , GRCh38.p12 chr7: 32,871,391-44,536,406	EPDR1, LOC107986734, 192 more genes
nsv3916442	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 37,309,607-48,670,880 , GRCh37 chr7: 37,343,082-48,700,334 , GRCh38 chr7: 37,303,478-48,660,738	EPDR1, LOC102724903, 204 more genes
nsv3912277	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 32,684,528-41,051,106 , GRCh37 chr7: 32,718,003-41,084,581 , GRCh38 chr7: 32,678,391-41,044,983	EPDR1, MATCAP2, 134 more genes
nsv3912038	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 35,460,776-42,013,800 , NCBI36 chr7: 35,466,911-42,019,924 , GRCh37 chr7: 35,500,386-42,053,399	EPDR1, INHBA-AS1, 110 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	EPDR1, 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	EPDR1, 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	EPDR1, 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	EPDR1, TRGV3, 2682 more genes
nsv3915802	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-41,915,483 , GRCh38 chr7: 54,185-41,875,885 , NCBI36 chr7: 149,268-41,882,008	EPDR1, RPL23AP52, 638 more genes
nsv3899194	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 11,048,840-52,863,626 , GRCh38.p12 chr7: 11,009,213-52,795,933	EPDR1, BRWD1P3, 590 more genes
nsv3917263	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 33,328,312-62,377,476 , GRCh37 chr7: 33,367,924-61,831,899 , NCBI36 chr7: 33,334,449-61,469,334	EPDR1, MIR4649, 444 more genes
nsv3898448	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 30,463,886-43,470,805 , GRCh38.p12 chr7: 30,424,270-43,431,206	EPDR1, INMT, 193 more genes
nsv3895187	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 37,213,108-40,255,122 , GRCh38.p12 chr7: 37,173,503-40,215,523	EPDR1, LOC107986785, 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	EPDR1, 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	EPDR1, ACHE, 1532 more genes
nsv6313670	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr7: 27,507,832-39,072,473 , GRCh38.p12 chr7: 27,468,213-39,032,873	EPDR1, ADCYAP1R1, 175 more genes
nsv6634332	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635	EPDR1, RRBP1P1, 2680 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 21

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Number of Variants: 20

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