prkag2[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
nsv6312331	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 151,478,218-151,483,647 , GRCh38.p12 chr7: 151,781,132-151,786,561	PRKAG2
nsv6312535	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr7: 151,372,486-151,372,743 , GRCh38.p12 chr7: 151,675,400-151,675,657	PRKAG2
nsv5564443	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 151,254,277-151,254,328 , GRCh38.p12 chr7: 151,557,191-151,557,242	PRKAG2
nsv3883548	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr7: 151,675,400-151,786,561 , GRCh37 chr7: 151,372,486-151,483,647	PRKAG2
nsv3894133	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 151,448,492-151,525,466 , GRCh38.p12 chr7: 151,751,406-151,828,380	PRKAG2, PRKAG2-AS2
nsv4451416	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 151,573,582-151,573,715 , GRCh38 chr7: 151,876,497-151,876,630	PRKAG2, PRKAG2-AS1
nsv4681500	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr7: 151,252,200-151,575,316 , GRCh38.p12 chr7: 151,555,114-151,878,231	PRKAG2, PRKAG2-AS1, 1 more genes
nsv7097493	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 151,478,218-151,573,705 , GRCh38.p12 chr7: 151,781,132-151,876,620	PRKAG2, PRKAG2-AS1, 1 more genes
nsv4683720	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 151,478,228-151,573,715 , GRCh38.p12 chr7: 151,781,142-151,876,630	PRKAG2, PRKAG2-AS1, 1 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	PRKAG2, RNU6-438P, 2682 more genes
nsv4675615	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620	PRKAG2, ATG9B, 603 more genes
nsv3915633	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 134,002,121-158,077,335 , GRCh38 chr7: 134,666,829-158,591,882 , GRCh37 chr7: 134,351,581-158,384,574	PRKAG2, MOXD2P, 561 more genes
nsv3897512	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 137,917,376-159,119,707 , GRCh38.p12 chr7: 138,232,630-159,327,017	PRKAG2, LOC105375548, 520 more genes
nsv3903590	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 140,133,025-158,982,771 , GRCh38.p12 chr7: 140,433,225-159,190,080	PRKAG2, LOC105375597, 468 more genes
nsv3910344	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 140,754,198-159,307,523 , GRCh37 chr7: 140,453,998-159,100,212 , NCBI36 chr7: 140,100,467-158,792,973	PRKAG2, LOC112268012, 461 more genes
nsv3905379	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 140,636,858-159,119,707 , GRCh38.p12 chr7: 140,937,058-159,327,017	PRKAG2, AGAP3, 459 more genes
nsv3919772	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 141,307,130-158,821,317 , GRCh37 chr7: 142,528,609-159,128,556 , GRCh38 chr7: 141,960,861-159,335,866	PRKAG2, LOC105375567, 429 more genes
nsv3904188	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 141,938,235-159,126,310 , GRCh38.p12 chr7: 142,288,582-159,333,620	PRKAG2, RBM33-DT, 423 more genes
nsv3915683	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 143,884,559-159,282,390 , GRCh37 chr7: 143,581,652-159,075,079 , NCBI36 chr7: 143,212,585-158,767,840	PRKAG2, FASTK, 280 more genes
nsv3907788	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 143,839,360-159,138,663 , GRCh38.p12 chr7: 144,142,267-159,335,973	PRKAG2, GIMAP1, 264 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 96

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Number of Variants: 20

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