psmd11[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
nsv3900445	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 30,805,795-30,814,479 , GRCh38.p12 chr17: 32,478,777-32,487,461	PSMD11, CDK5R1
nsv3906523	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 30,805,795-30,835,770 , GRCh38.p12 chr17: 32,478,777-32,508,752	PSMD11, MYO1D, 2 more genes
nsv3895405	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 30,809,455-30,835,770 , GRCh38.p12 chr17: 32,482,437-32,508,752	PSMD11, MYO1D, 2 more genes
nsv3902826	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 30,805,795-30,831,245 , GRCh38.p12 chr17: 32,478,777-32,504,227	PSMD11, MYO1D, 1 more genes
nsv3909834	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 30,809,455-30,832,175 , GRCh38.p12 chr17: 32,482,437-32,505,157	PSMD11, CDK5R1, 1 more genes
nsv3900049	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 30,805,795-30,827,688 , GRCh38.p12 chr17: 32,478,777-32,500,670	PSMD11, MYO1D, 1 more genes
nsv3893859	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 30,809,455-30,831,245 , GRCh38.p12 chr17: 32,482,437-32,504,227	PSMD11, MYO1D, 1 more genes
nsv7137216	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 30,572,862-35,843,988 , GRCh38.p12 chr17: 32,245,843-36,446,544	PSMD11, C17orf50, 117 more genes
nsv3919950	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 24,298,969-27,841,151 , GRCh37 chr17: 27,274,843-30,817,038 , GRCh38 chr17: 28,947,825-32,490,020	PSMD11, MIR365B, 105 more genes
nsv3895059	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,578,241-32,142,196 , GRCh38.p12 chr17: 31,251,223-33,815,177	PSMD11, RNU6-1134P, 48 more genes
nsv4729951	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,989,741-32,355,632 , GRCh38.p12 chr17: 31,662,722-34,028,613	PSMD11, RNA5SP437, 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	PSMD11, 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	PSMD11, 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	PSMD11, 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	PSMD11, 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	PSMD11, LOC105371922, 1855 more genes
nsv4457831	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395	PSMD11, LOC105371753, 474 more genes
nsv3972367	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr17: 25,403,446-31,685,464 , GRCh38.p12 chr17: 27,076,420-33,358,446	PSMD11, ASIC2, 190 more genes
nsv3900204	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 30,497,948-31,819,040 , GRCh38.p12 chr17: 32,170,929-33,492,022	PSMD11, RHBDL3, 17 more genes
nsv3894205	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 30,484,937-31,108,798 , GRCh38.p12 chr17: 32,157,918-32,781,780	PSMD11, UBL5P2, 12 more genes

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Items: 20

Number of Variants: 20

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