plxnb2[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
nsv7137080	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 50,276,656-50,277,243 , GRCh37 chr22: 50,715,085-50,715,672	PLXNB2
nsv3893588	copy number variation	1	nstd102	human	Benign	GRCh37 chr22: 50,682,728-50,724,648 , GRCh38.p12 chr22: 50,244,299-50,286,219	PLXNB2, MAPK12, 3 more genes
nsv3907079	copy number variation	1	nstd102	human	Benign	GRCh37 chr22: 50,684,747-50,724,648 , GRCh38.p12 chr22: 50,246,318-50,286,219	PLXNB2, MAPK12, 2 more genes
nsv3903193	copy number variation	1	nstd102	human	Benign	GRCh37 chr22: 50,684,771-50,724,504 , GRCh38.p12 chr22: 50,246,342-50,286,075	PLXNB2, HDAC10, 2 more genes
nsv3906203	copy number variation	1	nstd102	human	Benign	GRCh37 chr22: 50,684,772-50,721,495 , GRCh38.p12 chr22: 50,246,343-50,283,066	PLXNB2, MAPK12, 2 more genes
nsv3893151	copy number variation	1	nstd102	human	Benign	GRCh37 chr22: 50,688,348-50,721,495 , GRCh38.p12 chr22: 50,249,919-50,283,066	PLXNB2, MAPK12, 2 more genes
nsv3894798	copy number variation	1	nstd102	human	Benign	GRCh37 chr22: 50,697,119-50,715,271 , GRCh38.p12 chr22: 50,258,690-50,276,842	PLXNB2, MAPK11, 1 more genes
nsv3906388	copy number variation	1	nstd102	human	Benign	GRCh37 chr22: 50,699,625-50,714,616 , GRCh38.p12 chr22: 50,261,196-50,276,187	PLXNB2, MAPK12, 1 more genes
nsv3895794	copy number variation	1	nstd102	human	Benign	GRCh37 chr22: 50,699,625-50,713,409 , GRCh38.p12 chr22: 50,261,196-50,274,980	PLXNB2, MAPK12, 1 more genes
nsv3900214	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,151,555-51,195,728 , GRCh38.p12 chr22: 41,755,551-50,757,300	PLXNB2, TYMP, 218 more genes
nsv6290298	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,321,321-51,244,066 , GRCh38.p12 chr22: 41,925,317-50,805,638	PLXNB2, CERK, 212 more genes
nsv3912011	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 40,597,093-49,525,130 , GRCh38 chr22: 41,871,143-50,739,836 , GRCh37 chr22: 42,267,147-51,178,264	PLXNB2, TUBGCP6, 213 more genes
nsv5381149	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,333,802-51,195,728 , GRCh38.p12 chr22: 41,937,798-50,757,300	PLXNB2, WBP2NL, 210 more genes
nsv4351202	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,416,026-51,181,759 , GRCh38.p12 chr22: 42,020,022-50,743,331	PLXNB2, WBP2NL, 204 more genes
nsv3893572	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,441,918-51,197,838 , GRCh38.p12 chr22: 42,045,914-50,759,410	PLXNB2, CYP2D8P, 206 more genes
nsv3920027	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 42,433,752-50,738,932 , NCBI36 chr22: 41,159,702-49,524,226 , GRCh37 chr22: 42,829,758-51,177,360	PLXNB2, MIR6821, 187 more genes
nsv3909355	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,955,616-51,183,840 , GRCh38.p12 chr22: 42,559,610-50,745,412	PLXNB2, LOC101927499, 182 more genes
nsv6314059	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 42,972,719-51,197,838 , GRCh38.p12 chr22: 42,576,713-50,759,410	PLXNB2, TRABD, 181 more genes
nsv3897841	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 43,050,743-51,197,838 , GRCh38.p12 chr22: 42,654,737-50,759,410	PLXNB2, LINC00229, 176 more genes
nsv3905339	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 43,111,156-51,183,840 , GRCh38.p12 chr22: 42,715,150-50,745,412	PLXNB2, RPL5P34, 174 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 153

Page of 8

Number of Variants: 20

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Supplemental Content

Find related data

Search details

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