arhgef26[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3888835	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 153,774,569-153,845,137 , GRCh38.p12 chr3: 154,056,780-154,127,348	ARHGEF26, ARHGEF26-AS1
nsv3885679	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 153,571,286-153,915,723 , GRCh38.p12 chr3: 153,853,497-154,197,934	ARHGEF26, RPL21P42, 1 more genes
nsv3920460	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 155,395,373-155,577,567 , GRCh37.p13 chr3: 153,912,683-154,094,873 , GRCh38.p12 chr3: 154,194,894-154,377,084	ARHGEF26, GPR149, 3 more genes
nsv6290244	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334	ARHGEF26, LOC102724145, 273 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	ARHGEF26, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	ARHGEF26, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	ARHGEF26, RPL23AP49, 2875 more genes
nsv3918981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446	ARHGEF26, LINC02614, 1469 more genes
nsv6637156	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502	ARHGEF26, H1-10, 846 more genes
nsv3918692	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833	ARHGEF26, LOC105374179, 785 more genes
nsv3874894	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 142,995,020-192,997,215 , GRCh38.p12 chr3: 143,276,178-193,279,426	ARHGEF26, RNU6-901P, 673 more genes
nsv3918066	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 152,100,512-198,118,383 , NCBI36 chr3: 153,300,991-199,329,651 , GRCh37 chr3: 151,818,301-197,845,254	ARHGEF26, LOC105374260, 696 more genes
nsv3918784	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 147,160,353-178,240,319 , GRCh38 chr3: 147,442,566-178,522,531 , NCBI36 chr3: 148,643,043-179,723,013	ARHGEF26, LOC105374167, 394 more genes
nsv5381765	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911	ARHGEF26, MBNL1-AS1, 339 more genes
nsv4684209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822	ARHGEF26, MTAPP1, 339 more genes
nsv6290273	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 142,729,607-157,921,084 , GRCh38.p12 chr3: 143,010,765-158,203,295	ARHGEF26, LINC02066, 206 more genes
nsv6313678	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046	ARHGEF26, RNU6-901P, 229 more genes
nsv3922071	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr3: 152,629,894-156,319,129 , GRCh37 chr3: 151,147,204-154,836,435 , GRCh38 chr3: 151,429,416-155,118,646	ARHGEF26, AADAC, 42 more genes
nsv6313632	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 151,147,204-154,845,718 , GRCh38.p12 chr3: 151,429,416-155,127,929	ARHGEF26, LOC105374171, 42 more genes

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