adcy1[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
nsv3893552	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 45,603,629-45,614,476 , GRCh38.p12 chr7: 45,564,030-45,574,877	ADCY1
nsv3890355	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 45,613,779-45,614,442 , GRCh38.p12 chr7: 45,574,180-45,574,843	ADCY1
nsv3898804	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 45,613,779-45,614,376 , GRCh38.p12 chr7: 45,574,180-45,574,777	ADCY1
nsv3904328	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 45,613,779-45,614,289 , GRCh38.p12 chr7: 45,574,180-45,574,690	ADCY1
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	ADCY1, 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	ADCY1, LOC107986817, 2014 more genes
nsv3924054	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 40,573,756-56,174,815 , NCBI36 chr7: 40,540,281-56,142,309 , GRCh38 chr7: 40,534,157-56,107,122	ADCY1, VOPP1-DT, 229 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	ADCY1, LOC102724903, 204 more genes
nsv3911166	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 40,060,197-50,611,198 , NCBI36 chr7: 40,026,722-50,578,692 , GRCh38 chr7: 40,020,598-50,543,500	ADCY1, SUGCT, 155 more genes
nsv6313509	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 40,778,439-50,228,656 , GRCh38.p12 chr7: 40,738,840-50,189,060	ADCY1, LINC01447, 142 more genes
nsv3919937	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 44,571,949-53,699,760 , GRCh37 chr7: 44,611,548-53,767,453 , NCBI36 chr7: 44,578,073-53,734,947	ADCY1, LOC105375262, 106 more genes
nsv5381787	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,341,583-50,171,623 , GRCh38.p12 chr7: 43,301,984-50,132,027	ADCY1, OGDH, 110 more genes
nsv5381783	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 41,124,364-47,945,566 , GRCh38.p12 chr7: 41,084,766-47,905,969	ADCY1, ELK1P1, 121 more genes
nsv3896166	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 40,350,383-47,034,422 , GRCh38.p12 chr7: 40,310,784-46,994,824	ADCY1, LOC112267984, 118 more genes
nsv3915283	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 39,853,758-45,789,334 , GRCh38 chr7: 39,814,159-45,749,735 , NCBI36 chr7: 39,820,283-45,755,859	ADCY1, TUBG1P, 108 more genes
nsv3920348	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 44,232,968-46,597,979 , GRCh38 chr7: 44,193,369-46,558,381 , NCBI36 chr7: 44,199,493-46,564,504	ADCY1, CCM2, 50 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	ADCY1, 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	ADCY1, 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	ADCY1, 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	ADCY1, TRGV3, 2682 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 26

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Number of Variants: 20

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Supplemental Content

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Search details

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