dbVar for Gene (Select 80052) - 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
nsv7094683	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 65,821,800-72,146,396 , GRCh38.p12 chr16: 65,787,897-72,112,497	TRG-GCC5-1, RNU6-359P, 205 more genes
nsv7075094	inversion	1	nstd229	human		GRCh38 chr16: 67,913,190-69,541,641 , GRCh37.p13 chr16: 67,947,093-69,575,544	PSMB10, COG8, 52 more genes
nsv7075084	inversion	1	nstd229	human		GRCh38 chr16: 67,127,296-73,957,488 , GRCh37.p13 chr16: 67,161,199-73,991,387	MIR1538, LINC02136, 187 more genes
nsv7058675	inversion	1	nstd229	human		GRCh38 chr16: 67,667,666-75,720,241 , GRCh37.p13 chr16: 67,701,569-75,754,139	RNU6-898P, DPEP2, 199 more genes
nsv6996109	copy number variation	1	nstd229	human		GRCh38 chr16: 69,029,916-69,032,610 , GRCh37.p13 chr16: 69,063,819-69,066,513	TANGO6, RPS2P45
nsv6989204	copy number variation	1	nstd229	human		GRCh38 chr16: 69,032,944-69,039,125 , GRCh37.p13 chr16: 69,066,847-69,073,028	RPS2P45, TANGO6
nsv6981879	copy number variation	1	nstd229	human		GRCh38 chr16: 69,033,475-69,037,324 , GRCh37.p13 chr16: 69,067,378-69,071,227	TANGO6, RPS2P45
nsv6587327	inversion	1	nstd223	human		GRCh38 chr16: 69,031,933-69,032,909 , GRCh37.p13 chr16: 69,065,836-69,066,812	TANGO6, RPS2P45
nsv6513930	copy number variation	1	nstd223	human		GRCh38 chr16: 69,031,801-69,032,600 , GRCh37.p13 chr16: 69,065,704-69,066,503	RPS2P45, TANGO6
nsv6508352	copy number variation	1	nstd223	human		GRCh38 chr16: 69,009,330-69,099,250 , GRCh37.p13 chr16: 69,043,233-69,133,153	TANGO6, RPS2P45, 1 more genes
nsv6507314	copy number variation	1	nstd223	human		GRCh38 chr16: 69,029,861-69,032,632 , GRCh37.p13 chr16: 69,063,764-69,066,535	TANGO6, RPS2P45
nsv6315469	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 68,971,067-74,823,560 , GRCh38.p12 chr16: 68,937,164-74,789,662	ZNF19, RNU7-71P, 128 more genes
nsv6314755	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654	ATMIN, ATP6V0D1, 826 more genes
nsv6313976	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 68,850,677-69,377,553 , GRCh38.p12 chr16: 68,816,774-69,343,650	HAS3, LOC101060098, 17 more genes
nsv6133200	copy number variation	1	nstd213	human		GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395	, AARS1, 674 more genes
nsv6122384	copy number variation	1	nstd186	human		GRCh37 chr16: 69,063,655-69,066,508 , GRCh38.p12 chr16: 69,029,752-69,032,605	TANGO6, RPS2P45
nsv6022696	copy number variation	1	nstd212	human		GRCh38 chr16: 69,029,889-69,032,644 , GRCh37.p13 chr16: 69,063,792-69,066,547	RPS2P45, TANGO6
nsv5941235	copy number variation	1	nstd209	human		GRCh38 chr16: 69,029,861-69,032,631 , GRCh37.p13 chr16: 69,063,764-69,066,534	TANGO6, RPS2P45
nsv5871782	copy number variation	1	nstd209	human		GRCh38 chr16: 69,029,850-69,032,691 , GRCh37.p13 chr16: 69,063,753-69,066,594	TANGO6, RPS2P45
nsv5528628	copy number variation	1	nstd206	human		GRCh38 chr16: 69,029,752-69,032,605 , GRCh37.p13 chr16: 69,063,655-69,066,508	RPS2P45, TANGO6

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Number of Variants: 20

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Items: 1 to 20 of 137

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Number of Variants: 20

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