creb5[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
nsv3900719	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 28,574,339-28,576,766 , GRCh38.p12 chr7: 28,534,721-28,537,148	CREB5
nsv3897632	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 28,573,757-28,575,109 , GRCh38.p12 chr7: 28,534,139-28,535,491	CREB5
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	CREB5, 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	CREB5, LOC107986817, 2014 more genes
nsv3922885	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 20,561,456-32,005,143 , GRCh37 chr7: 20,601,079-32,044,755 , NCBI36 chr7: 20,567,604-32,011,280	CREB5, IL6-AS1, 195 more genes
nsv3892894	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 22,935,369-32,621,975 , GRCh38.p12 chr7: 22,895,750-32,582,363	CREB5, NPVF, 168 more genes
nsv4674822	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 23,877,135-33,139,446 , GRCh38.p12 chr7: 23,837,516-33,099,834	CREB5, RP9P, 156 more genes
nsv6315453	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 25,451,740-33,864,069 , GRCh38.p12 chr7: 25,412,121-33,824,457	CREB5, PLEKHA8, 141 more genes
nsv4435897	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 23,236,782-30,690,453 , GRCh38.p12 chr7: 23,197,163-30,650,837	CREB5, CCDC126, 138 more genes
nsv6636445	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 27,133,786-34,466,477 , GRCh38.p12 chr7: 27,094,167-34,426,865	CREB5, MIR550A1, 119 more genes
nsv3895202	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 24,344,104-28,879,357 , GRCh38.p12 chr7: 24,304,485-28,839,740	CREB5, HOXA10-HOXA9, 80 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	CREB5, 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	CREB5, 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	CREB5, 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	CREB5, 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	CREB5, 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	CREB5, BRWD1P3, 590 more genes
nsv3918785	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-37,129,317 , NCBI36 chr7: 149,268-37,095,842 , GRCh38 chr7: 54,185-37,089,712	CREB5, MMD2, 554 more genes
nsv3903410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 704,573-29,257,946 , GRCh38.p12 chr7: 664,936-29,218,330	CREB5, LOC100131264, 422 more genes
nsv3895449	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 11,562,624-36,395,416 , GRCh38.p12 chr7: 11,522,997-36,355,807	CREB5, HOXA7, 343 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 28

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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