arhgef10l[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
nsv3876852	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 17,872,028-17,903,298 , GRCh38.p12 chr1: 17,545,533-17,576,803	ARHGEF10L
nsv7098827	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749	ARHGEF10L, LOC107985467, 386 more genes
nsv3900501	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 3,006,193-17,688,934 , GRCh37 chr1: 2,922,757-18,015,429 , NCBI36 chr1: 2,912,617-17,888,016	ARHGEF10L, MFFP1, 364 more genes
nsv3900236	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 5,363,826-18,360,302 , GRCh37 chr1: 5,423,886-18,686,796 , NCBI36 chr1: 5,323,746-18,559,383	ARHGEF10L, PDPN, 333 more genes
nsv6636785	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 6,758,933-19,287,770 , GRCh38.p12 chr1: 6,698,873-18,961,276	ARHGEF10L, GPR157, 313 more genes
nsv6137724	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099	ARHGEF10L, PADI1, 176 more genes
nsv3899287	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 15,711,763-21,306,842 , NCBI36 chr1: 15,584,350-21,179,429 , GRCh38 chr1: 15,385,267-20,980,349	ARHGEF10L, EMC1-AS1, 166 more genes
nsv4728309	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 16,041,431-21,295,864 , GRCh38.p12 chr1: 15,714,936-20,969,371	ARHGEF10L, RNU1-6P, 150 more genes
nsv4728344	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 17,284,906-21,778,495 , GRCh38.p12 chr1: 16,958,411-21,452,002	ARHGEF10L, NBL1, 98 more genes
nsv3898082	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 16,008,307-19,988,832 , NCBI36 chr1: 15,880,894-19,861,419 , GRCh38 chr1: 15,681,812-19,662,339	ARHGEF10L, ESPNP, 114 more genes
nsv6290472	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 16,773,001-20,221,073 , GRCh38.p12 chr1: 16,446,506-19,894,580	ARHGEF10L, MIR1290, 92 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	ARHGEF10L, MARK1, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	ARHGEF10L, SNAP47, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	ARHGEF10L, RNU1-153P, 4887 more genes
nsv3909483	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 13,819,061-18,665,253 , GRCh38 chr1: 13,619,979-18,466,172 , GRCh37 chr1: 13,946,474-18,792,666	ARHGEF10L, TMEM51, 117 more genes
nsv3886392	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 18,016,160-18,632,174 , GRCh38.p12 chr1: 17,689,665-18,305,680	ARHGEF10L, IGSF21, 6 more genes
nsv4436181	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532	ARHGEF10L, LINC01776, 1853 more genes
nsv3887568	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 17,291,706-18,585,289 , GRCh38.p12 chr1: 16,965,211-18,258,795	ARHGEF10L, LINC02783, 20 more genes
nsv4436680	complex substitution	1	nstd102	human	Uncertain significance	GRCh38.p12 chr1: 973,858-24,379,779 , GRCh37 chr1: 909,238-24,706,269	ARHGEF10L, ALPL, 636 more genes
nsv4436486	complex substitution	1	nstd102	human	Uncertain significance	GRCh38.p12 chr1: 17,229,013-24,379,779 , GRCh37 chr1: 17,555,508-24,706,269	ARHGEF10L, ALPL, 174 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: 20

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity