dbVar for Gene (Select 23247) - 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
nsv7094831	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 27,561,492-27,733,036 , GRCh38.p12 chr16: 27,550,171-27,721,715	KATNIP, GTF3C1, 2 more genes
nsv7094778	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 27,712,890-27,713,036 , GRCh38.p12 chr16: 27,701,569-27,701,715	KATNIP
nsv7094777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 27,441,393-29,001,333 , GRCh38.p12 chr16: 27,430,072-28,990,012	NUPR1, RPS15AP33, 45 more genes
nsv7094776	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 27,441,393-28,899,063 , GRCh38.p12 chr16: 27,430,072-28,887,742	SH2B1, RNU6-1241P, 39 more genes
nsv6997999	copy number variation	1	nstd229	human		GRCh38 chr16: 27,585,269-27,585,295 , GRCh37.p13 chr16: 27,596,590-27,596,616	KATNIP
nsv6997893	copy number variation	1	nstd229	human		GRCh38 chr16: 27,730,903-27,734,404 , GRCh37.p13 chr16: 27,742,224-27,745,725	KATNIP
nsv6996824	copy number variation	1	nstd229	human		GRCh38 chr16: 27,604,395-27,607,264 , GRCh37.p13 chr16: 27,615,716-27,618,585	KATNIP
nsv6996170	copy number variation	1	nstd229	human		GRCh38 chr16: 27,670,578-27,924,224 , GRCh37.p13 chr16: 27,681,899-27,935,545	LOC100128079, GSG1L, 4 more genes
nsv6995581	copy number variation	1	nstd229	human		GRCh38 chr16: 27,553,709-27,553,743 , GRCh37.p13 chr16: 27,565,030-27,565,064	KATNIP
nsv6995225	copy number variation	1	nstd229	human		GRCh38 chr16: 27,577,393-27,653,434 , GRCh37.p13 chr16: 27,588,714-27,664,755	KATNIP
nsv6993665	copy number variation	1	nstd229	human		GRCh38 chr16: 27,710,651-27,712,956 , GRCh37.p13 chr16: 27,721,972-27,724,277	LOC100128079, KATNIP
nsv6993647	copy number variation	1	nstd229	human		GRCh38 chr16: 27,660,144-27,662,928 , GRCh37.p13 chr16: 27,671,465-27,674,249	KATNIP
nsv6993487	copy number variation	1	nstd229	human		GRCh38 chr16: 27,555,072-27,568,391 , GRCh37.p13 chr16: 27,566,393-27,579,712	KATNIP
nsv6992616	copy number variation	1	nstd229	human		GRCh38 chr16: 27,581,701-27,598,400 , GRCh37.p13 chr16: 27,593,022-27,609,721	KATNIP
nsv6991791	copy number variation	1	nstd229	human		GRCh38 chr16: 27,618,465-27,618,660 , GRCh37.p13 chr16: 27,629,786-27,629,981	KATNIP
nsv6991335	copy number variation	1	nstd229	human		GRCh38 chr16: 27,601,113-27,601,370 , GRCh37.p13 chr16: 27,612,434-27,612,691	KATNIP
nsv6991088	copy number variation	1	nstd229	human		GRCh38 chr16: 27,602,935-27,603,319 , GRCh37.p13 chr16: 27,614,256-27,614,640	KATNIP
nsv6991084	copy number variation	1	nstd229	human		GRCh38 chr16: 27,586,404-27,603,711 , GRCh37.p13 chr16: 27,597,725-27,615,032	KATNIP
nsv6991072	copy number variation	1	nstd229	human		GRCh38 chr16: 27,709,789-27,713,876 , GRCh37.p13 chr16: 27,721,110-27,725,197	LOC100128079, KATNIP

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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

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Subject Phenotype Status

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Items: 1 to 20 of 564

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Number of Variants: 20

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