kcnj2[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
nsv4769306	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 68,166,871-68,171,602 , GRCh38 chr17: 70,170,730-70,175,461	KCNJ2
nsv6310233	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr17: 68,171,181-68,172,464 , GRCh38.p12 chr17: 70,175,040-70,176,323	KCNJ2
nsv6290572	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr17: 70,166,313-70,176,696 , GRCh37.p13 chr17: 68,162,454-68,172,837	KCNJ2, KCNJ2-AS1
nsv3921648	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 68,090,109-68,705,937 , GRCh38 chr17: 70,093,968-70,709,796 , NCBI36 chr17: 65,601,704-66,217,532	KCNJ2, KCNJ16, 3 more genes
nsv3911811	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577	KCNJ2, PRPSAP1, 1350 more genes
nsv3910890	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 68,420,514-71,351,235 , NCBI36 chr17: 63,928,250-66,858,971 , GRCh37 chr17: 66,416,655-69,347,376	KCNJ2, KCNJ16, 34 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	KCNJ2, MIR3185, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	KCNJ2, P4HB, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	KCNJ2, MIR21, 2366 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	KCNJ2, SMURF2, 2366 more genes
nsv3914783	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577	KCNJ2, LOC105371922, 1855 more genes
nsv3909511	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846	KCNJ2, FOXK2, 958 more genes
nsv3913552	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225	KCNJ2, RNU6-131P, 1075 more genes
nsv4457646	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062	KCNJ2, LOC107985089, 448 more genes
nsv3909523	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 63,689,671-81,041,938 , GRCh38.p12 chr17: 65,693,553-83,084,062	KCNJ2, RPL38, 428 more genes
nsv3906075	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 67,002,415-81,041,938 , GRCh38.p12 chr17: 69,006,274-83,084,062	KCNJ2, CEP131, 374 more genes
nsv3917654	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 64,716,815-78,637,842 , GRCh37 chr17: 67,205,220-81,044,553 , GRCh38 chr17: 69,209,079-83,086,677	KCNJ2, LOC101928447, 368 more genes
nsv3919156	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 69,916,435-83,102,552 , GRCh37 chr17: 67,912,576-81,048,189 , NCBI36 chr17: 65,424,171-78,653,717	KCNJ2, CD300A, 359 more genes
nsv4676102	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr17: 68,056,381-68,268,736 , GRCh38.p12 chr17: 70,060,240-70,272,595	KCNJ2, KCNJ16, 5 more genes
nsv3972399	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr17: 64,159,738-74,891,024 , GRCh38.p12 chr17: 66,163,620-76,894,942	KCNJ2, AANAT, 243 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 25

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Number of Variants: 20

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Supplemental Content

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Search details

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