arhgap32[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4456479	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 129,050,108-129,103,417 , GRCh38.p12 chr11: 129,180,213-129,233,522	ARHGAP32, RNU6-874P, 1 more genes
nsv6314831	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr11: 128,939,186-129,086,991 , GRCh37.p13 chr11: 128,809,081-128,956,886	ARHGAP32, TP53AIP1, 1 more genes
nsv4457039	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 128,786,032-128,890,846 , GRCh38.p12 chr11: 128,916,137-129,020,951	ARHGAP32, TP53AIP1, 2 more genes
nsv3911009	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 119,424,297-135,075,271 , NCBI36 chr11: 118,800,217-134,450,377 , GRCh37 chr11: 119,295,007-134,945,165	ARHGAP32, PHB1P17, 304 more genes
nsv3922773	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 119,304,619-134,868,407 , GRCh38 chr11: 119,433,909-134,998,513 , NCBI36 chr11: 118,809,829-134,373,617	ARHGAP32, ETS1-AS1, 301 more genes
nsv3906843	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 119,538,664-134,938,470 , GRCh38.p12 chr11: 119,667,954-135,068,576	ARHGAP32, TMEM225, 296 more genes
nsv3902675	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 119,807,473-134,868,407 , GRCh38.p12 chr11: 119,936,764-134,998,513	ARHGAP32, FEZ1, 291 more genes
nsv3923251	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 119,891,678-134,450,377 , GRCh38 chr11: 120,515,759-135,075,271 , GRCh37 chr11: 120,386,468-134,945,165	ARHGAP32, KIRREL3-AS3, 279 more genes
nsv3901752	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 120,527,021-134,938,470 , GRCh38.p12 chr11: 120,656,312-135,068,576	ARHGAP32, LOC105369534, 276 more genes
nsv4436748	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 120,576,984-134,934,063 , GRCh38.p12 chr11: 120,706,275-135,064,169	ARHGAP32, LINC02098, 276 more genes
nsv3904760	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 120,615,374-134,868,407 , GRCh38.p12 chr11: 120,744,665-134,998,513	ARHGAP32, OR8D2, 275 more genes
nsv4675832	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 120,742,540-134,938,470 , GRCh38.p12 chr11: 120,871,831-135,068,576	ARHGAP32, MIR8052, 275 more genes
nsv3924566	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 120,507,265-134,576,266 , NCBI36 chr11: 119,883,184-133,951,370 , GRCh37 chr11: 120,377,974-134,446,160	ARHGAP32, CCDC15-DT, 271 more genes
nsv3891701	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 121,136,603-134,938,470 , GRCh38.p12 chr11: 121,265,894-135,068,576	ARHGAP32, OR10G9, 266 more genes
nsv7137129	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659	ARHGAP32, VSIG10L2, 268 more genes
nsv3895234	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 121,416,261-134,938,470 , GRCh38.p12 chr11: 121,545,552-135,068,576	ARHGAP32, SF3A3P2, 262 more genes
nsv3918400	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 121,482,185-134,938,470 , GRCh38 chr11: 121,611,476-135,068,576 , NCBI36 chr11: 120,987,395-134,443,680	ARHGAP32, RN7SL167P, 262 more genes
nsv3915295	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 121,064,970-134,450,377 , GRCh38 chr11: 121,689,052-135,075,271 , GRCh37 chr11: 121,559,760-134,945,165	ARHGAP32, LOC105369591, 262 more genes
nsv3892434	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 121,501,072-134,868,348 , GRCh38.p12 chr11: 121,630,363-134,998,454	ARHGAP32, ZNF123P, 261 more genes
nsv3919969	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 121,780,459-135,075,271 , GRCh37 chr11: 121,651,167-134,945,165 , NCBI36 chr11: 121,156,377-134,450,377	ARHGAP32, STT3A-AS1, 262 more genes

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

Send to:

Search results

Items: 1 to 20 of 90

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

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 90

Page of 5

Number of Variants: 20

Page of 5

Supplemental Content

Find related data

Search details

Recent activity