dbVar for Gene (Select 54920) - 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
nsv7060255	inversion	1	nstd229	human		GRCh38 chr16: 67,996,909-68,021,294 , GRCh37.p13 chr16: 68,030,812-68,055,197	KARS1P3, DUS2, 4 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
nsv6996974	copy number variation	1	nstd229	human		GRCh38 chr16: 68,042,785-68,106,725 , GRCh37.p13 chr16: 68,076,688-68,140,628	NFATC3, DUS2
nsv6995698	copy number variation	1	nstd229	human		GRCh38 chr16: 68,056,519-68,062,701 , GRCh37.p13 chr16: 68,090,422-68,096,604	DUS2
nsv6995396	copy number variation	1	nstd229	human		GRCh38 chr16: 68,028,306-68,028,972 , GRCh37.p13 chr16: 68,062,209-68,062,875	DUS2
nsv6993050	copy number variation	1	nstd229	human		GRCh38 chr16: 68,022,246-68,030,000 , GRCh37.p13 chr16: 68,056,149-68,063,903	DUS2, DDX28
nsv6991134	copy number variation	1	nstd229	human		GRCh38 chr16: 68,079,743-68,084,900 , GRCh37.p13 chr16: 68,113,646-68,118,803	NFATC3, DUS2
nsv6990366	copy number variation	1	nstd229	human		GRCh38 chr16: 68,044,501-68,046,300 , GRCh37.p13 chr16: 68,078,404-68,080,203	DUS2
nsv6989018	copy number variation	1	nstd229	human		GRCh38 chr16: 68,027,780-68,029,227 , GRCh37.p13 chr16: 68,061,683-68,063,130	DUS2
nsv6987867	copy number variation	1	nstd229	human		GRCh38 chr16: 67,764,668-68,219,679 , GRCh37.p13 chr16: 67,798,571-68,253,582	DDX28, NUTF2, 19 more genes
nsv6984442	copy number variation	1	nstd229	human		GRCh38 chr16: 68,001,921-68,036,383 , GRCh37.p13 chr16: 68,035,824-68,070,286	RNU6-359P, KARS1P3, 3 more genes
nsv6980304	copy number variation	1	nstd229	human		GRCh38 chr16: 68,029,853-68,038,950 , GRCh37.p13 chr16: 68,063,756-68,072,853	DUS2
nsv6623489	copy number variation	1	nstd224	human		GRCh37 chr16: 67,943,050-68,068,627 , GRCh38.p12 chr16: 67,909,147-68,034,724	DPEP2NB, PSKH1, 10 more genes
nsv6575705	inversion	1	nstd223	human		GRCh38 chr16: 68,042,726-68,043,201 , GRCh37.p13 chr16: 68,076,629-68,077,104	DUS2
nsv6512423	copy number variation	1	nstd223	human		GRCh38 chr16: 68,026,443-68,028,932 , GRCh37.p13 chr16: 68,060,346-68,062,835	DUS2
nsv6512184	copy number variation	1	nstd223	human		GRCh38 chr16: 68,023,996-68,030,371 , GRCh37.p13 chr16: 68,057,899-68,064,274	DUS2
nsv6511160	copy number variation	1	nstd223	human		GRCh38 chr16: 68,027,780-68,029,225 , GRCh37.p13 chr16: 68,061,683-68,063,128	DUS2

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Number of Variants: 20

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Items: 1 to 20 of 281

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Number of Variants: 20

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