dbVar for Gene (Select 286094) - 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
nsv5491227	copy number variation	1	nstd206	human		GRCh38 chr8: 135,288,207-135,291,598 , GRCh37.p13 chr8: 136,300,450-136,303,841	LINC01591
nsv4962331	copy number variation	1	nstd200	human		GRCh38 chr8: 135,282,170-135,282,257 , GRCh37.p13 chr8: 136,294,413-136,294,500	LINC01591
nsv4675664	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 128,877,995-146,295,771 , GRCh38.p12 chr8: 127,865,749-145,070,385	LOC105375789, LINC02990, 270 more genes
nsv4675273	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 121,042,467-146,295,771 , GRCh38.p12 chr8: 120,030,228-145,070,385	TOP1MT, SLA, 379 more genes
nsv4674996	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 126,892,814-143,750,028 , GRCh38.p12 chr8: 125,880,570-142,668,610	POU5F1B, DNAJC8P3, 158 more genes
nsv4617438	copy number variation	1	nstd183	human		GRCh37 chr8: 136,264,512-136,277,550 , GRCh38.p12 chr8: 135,252,269-135,265,307	LINC01591
nsv4492515	mobile element insertion	1	nstd166	human		GRCh37.p13 chr8: 136,310,824-136,310,824 , GRCh38.p12 chr8: 135,298,581-135,298,581	LINC01591
nsv4456997	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 125,496,223-146,295,771 , GRCh38.p12 chr8: 124,483,982-145,070,385	LOC107986906, GPIHBP1, 317 more genes
nsv4456811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385	TERF1, LOC107986945, 1511 more genes
nsv4456783	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 122,193,546-146,295,771 , GRCh38.p12 chr8: 121,181,306-145,070,385	HAS2, ZNF696, 369 more genes
nsv4455524	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 136,059,859-146,295,771 , GRCh38.p12 chr8: 135,047,616-145,070,385	LINC00051, LOC107986982, 197 more genes
nsv4349554	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385	LOC101929488, TEX15, 2105 more genes
nsv4155971	copy number variation	1	nstd166	human		GRCh37.p13 chr8: 136,281,964-136,282,023 , GRCh38.p12 chr8: 135,269,721-135,269,780	LINC01591
nsv3924568	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 131,720,610-146,264,902 , GRCh38 chr8: 130,639,182-145,068,712 , GRCh37 chr8: 131,651,428-146,294,098	MAFA-AS1, DENND3-AS1, 244 more genes
nsv3924437	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr8: 135,967,800-136,878,391 , GRCh37 chr8: 135,898,618-136,809,209 , GRCh38 chr8: 134,886,375-135,796,966	KHDRBS3, LOC101927872, 4 more genes
nsv3923310	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098	LOC112268023, RPL23AP96, 2105 more genes
nsv3922201	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 129,302,340-146,245,639 , GRCh38 chr8: 128,220,912-145,049,449 , GRCh37 chr8: 129,233,158-146,274,835	CYP11B2, SLC45A4-AS1, 261 more genes
nsv3921784	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 131,196,946-142,307,491 , GRCh38 chr8: 130,115,518-141,228,210 , GRCh37 chr8: 131,127,764-142,238,309	MTND2P7, HPYR1, 86 more genes
nsv3920738	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 113,580,402-145,054,634 , NCBI36 chr8: 114,661,807-146,250,824 , GRCh37 chr8: 114,592,631-146,280,020	KHDRBS3, DENND3-AS1, 438 more genes
nsv3919841	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 78,614,077-145,054,634 , GRCh37 chr8: 79,526,312-146,280,020 , NCBI36 chr8: 79,688,867-146,250,824	LY6S-AS1, LOC107984017, 911 more genes

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Number of Variants: 20

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Result Filters

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Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 211

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Number of Variants: 20

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