dbVar for Gene (Select 79006) - 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
nsv7094666	copy number variation	3	nstd102	human	Uncertain significance	GRCh37 chr16: 256,302-4,852,572 , GRCh38.p12 chr16: 206,303-4,802,571	DNAAF8, TMEM204, 282 more genes
nsv7094665	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 256,302-1,918,176 , GRCh38.p12 chr16: 206,303-1,868,175	MRPS34, LOC105371044, 97 more genes
nsv7094664	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 256,302-1,843,653 , GRCh38.p12 chr16: 206,303-1,793,652	NME4, UNKL, 94 more genes
nsv7094663	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 256,302-1,657,267 , GRCh38.p12 chr16: 206,303-1,607,266	TPSP2, PRR25, 83 more genes
nsv7064153	inversion	1	nstd229	human		GRCh38 chr16: 463,012-758,884 , GRCh37.p13 chr16: 513,012-808,884	LINC00235, ANTKMT, 27 more genes
nsv6975395	copy number variation	1	nstd229	human		GRCh38 chr16: 715,812-718,064 , GRCh37.p13 chr16: 765,812-768,064	METRN
nsv6959924	copy number variation	1	nstd229	human		GRCh38 chr16: 705,631-733,513 , GRCh37.p13 chr16: 755,631-783,513	FBXL16, METRN, 4 more genes
nsv6637972	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,881-1,350,186 , GRCh38.p12 chr16: 35,881-1,300,185	MPG, LOC105371038, 78 more genes
nsv6637644	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 726,789-1,066,511 , GRCh38.p12 chr16: 676,789-1,016,511	WDR24, STUB1, 21 more genes
nsv6634427	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 111,043-6,627,459 , GRCh38.p12 chr16: 61,045-6,577,458	HBA1, ANTKMT, 312 more genes
nsv6314105	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-1,468,828 , GRCh38.p12 chr16: 35,880-1,418,827	HBA2, LUC7L, 87 more genes
nsv6133278	copy number variation	2	nstd213	human		GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144	, ABAT, 446 more genes
nsv6133001	copy number variation	1	nstd213	human		GRCh37 chr16: 770,000-890,001 , GRCh38.p12 chr16: 720,000-840,001	MSLN, GNG13, 10 more genes
nsv6112797	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012	ANTKMT, HBA1, 307 more genes
nsv5929553	copy number variation	1	nstd209	human		GRCh38 chr16: 718,548-718,631 , GRCh37.p13 chr16: 768,548-768,631	ANTKMT, METRN
nsv5380998	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr16: 624,055-2,153,916 , GRCh38.p12 chr16: 574,055-2,103,915	NDUFB10, BAIAP3, 102 more genes
nsv5380784	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 765,584-1,204,036 , GRCh38.p12 chr16: 715,584-1,154,036	LOC105371042, CCDC78, 21 more genes
nsv5279314	copy number variation	1	nstd204	human		GRCh38.p13 chr16: 631,501-737,100 , GRCh37.p13 chr16: 681,501-787,100	, CIAO3, 18 more genes
nsv5278593	copy number variation	1	nstd204	human		GRCh38.p13 chr16: 495,101-1,599,500 , GRCh37.p13 chr16: 545,101-1,649,501	, MIR662, 73 more genes
nsv5265522	copy number variation	1	nstd204	human		GRCh38.p13 chr16: 53,201-2,576,200 , GRCh37.p13 chr16: 103,201-2,626,201	, RHBDL1, 175 more genes

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Number of Variants: 20

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Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 472

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Number of Variants: 20

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