dbVar for Gene (Select 8733) - 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
nsv5720680	mobile element insertion	1	nstd211	human		GRCh38 chr8: 144,081,639-144,081,639 , GRCh37.p13 chr8: 145,136,542-145,136,542 , GRCh37.p13 chr8\|NW_003315923.1: 420,286-420,286	GPAA1
nsv5381643	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 145,047,561-145,701,149 , GRCh38.p12 chr8: 143,973,393-144,475,766	ZFTRAF1, DGAT1, 40 more genes
nsv5248548	copy number variation	1	nstd204	human		GRCh38.p13 chr8: 143,866,301-144,531,400 , GRCh37.p13 chr8: 145,146,063-145,756,784	MIR661, EXOSC4, 51 more genes
nsv5189113	mobile element insertion	1	nstd203	human		GRCh38 chr8: 144,081,639-144,081,649 , GRCh37.p13 chr8: 145,136,542-145,136,552 , GRCh37.p13 chr8\|NW_003315923.1: 420,286-420,296	GPAA1
nsv4769373	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 145,033,244-146,297,937 , GRCh38.p12 chr8: 143,959,076-145,072,551	ZFTRAF1, PLEC, 68 more genes
nsv4729603	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr8: 144,262,042-146,295,771 , GRCh38.p12 chr8: 143,180,625-145,070,385	CYC1, EEF1D, 112 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
nsv4675029	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 142,132,678-145,569,441 , GRCh38.p12 chr8: 141,122,579-144,345,779	RHPN1-AS1, MIR6847, 117 more genes
nsv4605974	copy number variation	1	nstd183	human		GRCh37 chr8: 145,138,077-145,138,230 , GRCh38.p12 chr8: 144,083,174-144,083,327	GPAA1
nsv4557910	mobile element insertion	1	nstd166	human		GRCh37.p13 chr8: 145,136,542-145,136,542 , GRCh38.p12 chr8: 144,081,639-144,081,639	GPAA1
nsv4457078	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 139,188,797-146,295,771 , GRCh38.p12 chr8: 138,176,554-145,070,385	GSDMD, MROH1, 181 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
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
nsv4455260	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 144,190,206-146,295,771 , GRCh38.p12 chr8: 143,108,789-145,070,385	COMMD5, RHPN1-AS1, 113 more genes
nsv4454506	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 144,990,335-145,701,149 , GRCh38.p12 chr8: 143,916,167-144,475,766	SCRT1, MIR7112, 41 more genes
nsv4449773	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 144,990,325-145,700,664 , GRCh38.p12 chr8: 143,916,157-144,475,281	FOXH1, MIR10400, 41 more genes
nsv4349929	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 144,879,444-145,199,846 , GRCh38.p12 chr8: 143,797,274-144,144,943	TSSK5P, HGH1, 22 more genes

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Has Clinical Interpretation

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Items: 1 to 20 of 281

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Number of Variants: 20

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