arhgap10[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
nsv3875096	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 148,848,283-148,952,982 , GRCh38.p12 chr4: 147,927,132-148,031,831	ARHGAP10
nsv3897951	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 24,847,361-24,870,596 , GRCh38.p12 chr10: 24,558,432-24,581,667	ARHGAP21
nsv5200368	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 148,911,418-149,103,259 , GRCh38.p12 chr4: 147,990,267-148,182,108	ARHGAP10, NR3C2
nsv3880126	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 148,916,436-149,103,774 , GRCh38.p12 chr4: 147,995,285-148,182,623	ARHGAP10, NR3C2
nsv6636538	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 148,734,569-148,860,556 , GRCh38.p12 chr4: 147,813,418-147,939,405	ARHGAP10, RFPL4AP4
nsv3878113	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 148,765,966-148,840,301 , GRCh38.p12 chr4: 147,844,815-147,919,150	ARHGAP10, RFPL4AP4
nsv3913425	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr4: 149,061,552-149,497,087 , GRCh37 chr4: 148,842,102-149,277,637 , GRCh38 chr4: 147,920,951-148,356,485	ARHGAP10, NR3C2, 1 more genes
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	RNU7-12P, RNU1-65P, 1876 more genes
nsv3923320	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 144,509,997-149,435,179 , NCBI36 chr4: 144,729,447-149,654,629 , GRCh38 chr4: 143,588,844-148,514,027	ARHGAP10, FREM3, 62 more genes
nsv4455223	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 146,118,793-150,492,144 , GRCh38.p12 chr4: 145,197,641-149,570,992	ARHGAP10, SMAD1-AS1, 56 more genes
nsv6311715	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 146,560,292-149,358,012 , GRCh38.p12 chr4: 145,639,140-148,436,860	ARHGAP10, PRMT5P1, 32 more genes
nsv3910612	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 24,400,270-25,639,569 , GRCh38 chr10: 24,111,341-25,350,640 , NCBI36 chr10: 24,440,276-25,679,575	ARHGAP21, KIAA1217, 13 more genes
nsv3873978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724	ARHGAP10, LOC100422029, 2358 more genes
nsv3876533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611	ARHGAP10, LOC100420289, 2347 more genes
nsv3884499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286	ARHGAP10, MTND4LP29, 2341 more genes
nsv3880085	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318	ARHGAP10, LOC112268460, 2345 more genes
nsv3883791	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495	ARHGAP10, LOC105377343, 2341 more genes
nsv3906389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996	LOC100419870, LOC102724439, 2105 more genes
nsv3891157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558	AGAP14P, LOC100505502, 2097 more genes
nsv3902271	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639	ANXA11, EDRF1-DT, 2085 more genes

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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 58

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Number of Variants: 20

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