dbVar for Gene (Select 84264) - 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
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
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
nsv5263615	copy number variation	1	nstd204	human		GRCh38.p13 chr16: 504,601-857,400 , GRCh37.p13 chr16: 554,601-907,400	, LINC00235, 36 more genes
nsv4866310	copy number variation	1	nstd200	human		GRCh37 chr16: 776,875-777,195 , GRCh38.p12 chr16: 726,875-727,195	HAGHL, CCDC78
nsv4729241	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456	MTRNR2L4, BRICD5, 307 more genes
nsv4683390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 624,055-2,148,005 , GRCh38.p12 chr16: 574,055-2,098,004	MRPS34, HAGHL, 102 more genes
nsv4682518	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 624,055-2,550,979 , GRCh38.p12 chr16: 574,055-2,500,978	C1QTNF8, NHERF2, 133 more genes
nsv4681479	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 772,760-776,377 , GRCh38.p12 chr16: 722,760-726,377	HAGHL, ANTKMT, 1 more genes
nsv4676068	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-1,166,355 , GRCh38.p12 chr16: 35,880-1,116,355	LINC00235, C1QTNF8, 69 more genes
nsv4675066	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 364,182-1,186,480 , GRCh38.p12 chr16: 314,182-1,136,480	SOX8, LMF1-AS1, 50 more genes
nsv4630782	copy number variation	1	nstd183	human		GRCh37 chr16: 778,094-778,157 , GRCh38.p12 chr16: 728,094-728,157	HAGHL, CIAO3
nsv4625516	copy number variation	1	nstd183	human		GRCh37 chr16: 777,100-779,633 , GRCh38.p12 chr16: 727,100-729,633	CCDC78, HAGHL, 1 more genes
nsv4457133	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-830,613 , GRCh38.p12 chr16: 35,880-780,613	IL9RP3, HBZ, 56 more genes
nsv4455728	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-1,468,459 , GRCh38.p12 chr16: 35,880-1,418,458	GNG13, LOC100134368, 87 more genes
nsv4455594	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-2,053,328 , GRCh38.p12 chr16: 35,880-2,003,327	JPT2, TSR3, 128 more genes
nsv4449893	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 624,055-2,115,656 , GRCh38.p12 chr16: 574,055-2,065,655	LMF1-AS1, RAB40C, 99 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Links from Gene

Items: 1 to 20 of 462

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Number of Variants: 20

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Recent activity