ARHGAP5-AS1 - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6943079	copy number variation	1	nstd229	human		GRCh38 chr14: 32,068,129-32,089,427 , GRCh37.p13 chr14: 32,537,335-32,558,633	ARHGAP5-AS1, ARHGAP5
nsv4224354	copy number variation	1	nstd166	human		GRCh37.p13 chr14: 32,542,447-32,545,670 , GRCh38.p12 chr14: 32,073,241-32,076,464	ARHGAP5-AS1, ARHGAP5
esv3359965	copy number variation	8	estd59	human		NCBI36 chr14: 31,614,977-31,617,825 , GRCh37.p13 chr14: 32,545,226-32,548,074 , GRCh38.p12 chr14: 32,076,020-32,078,868	ARHGAP5-AS1, ARHGAP5
nsv1777609	short tandem repeat	2	nstd128	human		GRCh37 chr14: 32,546,164-32,546,179 , GRCh38.p12 chr14: 32,076,958-32,076,973	ARHGAP5-AS1, ARHGAP5
nsv1765232	short tandem repeat	4	nstd128	human		GRCh37 chr14: 32,543,795-32,543,808 , GRCh38.p12 chr14: 32,074,589-32,074,602	ARHGAP5-AS1, ARHGAP5
nsv1765609	short tandem repeat	1	nstd128	human		GRCh37 chr14: 32,543,392-32,543,404 , GRCh38.p12 chr14: 32,074,186-32,074,198	ARHGAP5-AS1, ARHGAP5
nsv6132587	copy number variation	1	nstd213	human		GRCh37 chr14: 32,210,000-32,640,001 , GRCh38.p12 chr14: 31,740,794-32,170,795	ARHGAP5-AS1, ARHGAP5, 3 more genes
nsv4529189	copy number variation	1	nstd166	human		GRCh37.p13 chr14: 32,232,999-32,571,000 , GRCh38.p12 chr14: 31,763,793-32,101,794	ARHGAP5-AS1, NUBPL, 3 more genes
esv3809442	tandem duplication	1	estd192	human		GRCh37 chr14: 32,511,575-32,546,749 , GRCh38.p12 chr14: 32,042,369-32,077,543	ARHGAP5-AS1, LOC105370440, 1 more genes
nsv6314715	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884	ARHGAP5-AS1, HNRNPC, 616 more genes
nsv3916277	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 19,734,944-44,823,755 , GRCh38 chr14: 20,196,945-45,284,802 , GRCh37 chr14: 20,665,104-45,754,005	ARHGAP5-AS1, MIR208B, 600 more genes
nsv3917157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 24,018,169-42,452,605 , GRCh38 chr14: 23,548,960-41,983,402 , NCBI36 chr14: 23,088,009-41,522,355	ARHGAP5-AS1, LINC02300, 274 more genes
nsv3924751	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 31,261,477-45,154,334 , GRCh38 chr14: 30,792,271-44,685,131 , NCBI36 chr14: 30,331,228-44,224,084	ARHGAP5-AS1, DNAJC8P1, 171 more genes
nsv6637416	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 24,959,823-33,415,359 , GRCh38.p12 chr14: 24,490,617-32,946,153	ARHGAP5-AS1, SCFD1, 94 more genes
nsv3922917	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 30,851,760-38,181,546 , NCBI36 chr14: 29,921,511-37,251,297 , GRCh38 chr14: 30,382,554-37,712,341	ARHGAP5-AS1, MBIP, 124 more genes
nsv4457320	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 30,448,939-35,017,859 , GRCh38.p12 chr14: 29,979,733-34,548,653	ARHGAP5-AS1, NARS1P1, 56 more genes
nsv3911062	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 29,273,194-33,703,472 , NCBI36 chr14: 28,342,945-32,773,223 , GRCh38 chr14: 28,803,988-33,234,266	ARHGAP5-AS1, HEATR5A, 54 more genes
nsv3902883	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863	ARHGAP5-AS1, LOC440181, 1998 more genes
nsv3907460	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456	ARHGAP5-AS1, BANF1P1, 1996 more genes
nsv3899639	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456	ARHGAP5-AS1, LOC100289511, 1996 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 93

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 93

Page of 5

Number of Variants: 20

Page of 5

Supplemental Content

Find related data

Search details

Recent activity