dbVar for Gene (Select 93668) - 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
nsv5912093	copy number variation	1	nstd209	human		GRCh38 chr8: 132,561,032-132,570,197 , GRCh37.p13 chr8: 133,573,279-133,582,445	DNAAF11, HPYR1
nsv5865999	copy number variation	1	nstd209	human		GRCh38 chr8: 132,561,021-132,570,100 , GRCh37.p13 chr8: 133,573,268-133,582,348	HPYR1, DNAAF11
nsv5673945	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr8: 133,141,509-134,296,554 , GRCh38.p12 chr8: 132,129,262-133,284,311	SLA, TMEM71, 15 more genes
nsv5479594	copy number variation	1	nstd206	human		GRCh38 chr8: 132,544,216-132,574,422 , GRCh37.p13 chr8: 133,556,463-133,586,670	HPYR1, DNAAF11
nsv4729309	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 133,176,537-133,891,988 , GRCh38.p12 chr8: 132,164,290-132,879,743	LOC105375767, KCNQ3, 6 more genes
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
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
nsv4456266	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 131,915,430-135,240,074 , GRCh38.p12 chr8: 130,903,184-134,227,831	LOC105375772, KCNQ3, 36 more genes
nsv4455511	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 124,120,772-135,265,846 , GRCh38.p12 chr8: 123,108,532-134,253,603	MTSS1, PCAT2, 148 more genes
nsv4452863	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 133,141,489-134,296,574 , GRCh38.p12 chr8: 132,129,242-133,284,331	LOC105375769, MIR7848, 15 more genes
nsv4387110	copy number variation	1	nstd173	human		GRCh37 chr8: 130,922,524-135,867,123 , GRCh38.p12 chr8: 129,910,278-134,854,880	, NDRG1, 53 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
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
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

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Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 166

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Number of Variants: 20

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