dbVar for Gene (Select 162083) - 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
nsv7137115	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 21,467,726-29,044,717 , GRCh38.p12 chr16: 21,456,405-29,033,396	OTOAP1, GGA2, 148 more genes
nsv6992078	copy number variation	1	nstd229	human		GRCh38 chr16: 26,975,134-27,204,892 , GRCh37.p13 chr16: 26,986,455-27,216,213	KDM8, LOC105371154, 4 more genes
nsv6991765	copy number variation	1	nstd229	human		GRCh38 chr16: 27,053,596-27,066,331 , GRCh37.p13 chr16: 27,064,917-27,077,652	C16orf82, LOC105371154
nsv6987821	copy number variation	1	nstd229	human		GRCh38 chr16: 27,041,641-27,077,648 , GRCh37.p13 chr16: 27,052,962-27,088,969	C16orf82, LOC105371153, 1 more genes
nsv6984493	copy number variation	1	nstd229	human		GRCh38 chr16: 26,445,367-27,411,745 , GRCh37.p13 chr16: 26,456,688-27,423,066	LOC105371153, KDM8, 9 more genes
nsv6979529	copy number variation	1	nstd229	human		GRCh38 chr16: 27,063,927-27,066,738 , GRCh37.p13 chr16: 27,075,248-27,078,059	C16orf82
nsv6979322	copy number variation	1	nstd229	human		GRCh38 chr16: 27,046,185-27,097,651 , GRCh37.p13 chr16: 27,057,506-27,108,972	C16orf82, LOC105371153, 1 more genes
nsv6637633	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 21,576,803-30,177,240 , GRCh38.p12 chr16: 21,565,482-30,165,919	USP31, CA5AP1, 200 more genes
nsv6637429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029	MIR6511B2, ACSM5, 535 more genes
nsv6623390	copy number variation	1	nstd224	human		GRCh37 chr16: 27,078,433-27,090,311 , GRCh38.p12 chr16: 27,067,112-27,078,990	C16orf82
nsv6623389	copy number variation	1	nstd224	human		GRCh37 chr16: 27,078,327-27,093,137 , GRCh38.p12 chr16: 27,067,006-27,081,816	C16orf82
nsv6290289	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 21,594,997-29,625,302 , GRCh38.p12 chr16: 21,583,676-29,613,981	LOC105371149, SLX1B, 166 more genes
nsv6289847	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 21,530,207-29,332,245 , GRCh38.p12 chr16: 21,518,886-29,320,924	GAPDHP35, NSMCE1, 154 more genes
nsv6133268	copy number variation	1	nstd213	human		GRCh37 chr16: 22,710,000-32,010,001 , GRCh38.p12 chr16: 22,698,679-31,998,680	ALDOA, AQP8, 269 more genes
nsv6133267	copy number variation	1	nstd213	human		GRCh37 chr16: 22,710,000-30,200,001 , GRCh38.p12 chr16: 22,698,679-30,188,680	ALDOA, AQP8, 169 more genes
nsv5522856	copy number variation	1	nstd206	human		GRCh38 chr16: 27,041,641-27,077,648 , GRCh37.p13 chr16: 27,052,962-27,088,969	LOC105371154, C16orf82, 1 more genes
nsv5515970	copy number variation	1	nstd206	human		GRCh38 chr16: 27,065,688-27,087,463 , GRCh37.p13 chr16: 27,077,009-27,098,784	C16orf82
nsv5303373	copy number variation	1	nstd204	human		GRCh38.p13 chr16: 27,065,217-27,065,498 , GRCh37.p13 chr16: 27,076,538-27,076,819	C16orf82
nsv4994588	copy number variation	1	nstd200	human		GRCh38 chr16: 27,041,641-27,077,648 , GRCh37.p13 chr16: 27,052,962-27,088,969	LOC105371154, LOC105371153, 1 more genes
nsv4864087	copy number variation	1	nstd200	human		GRCh37 chr16: 27,052,962-27,088,969 , GRCh38.p12 chr16: 27,041,641-27,077,648	LOC105371154, C16orf82, 1 more genes

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Items: 1 to 20 of 136

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Number of Variants: 20

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