dbVar for Gene (Select 339123) - 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
nsv7145999	copy number variation	1	nstd232	human		GRCh37.p13 chr16: 732,275-732,356 , GRCh38.p12 chr16: 682,275-682,356	STUB1, JMJD8
nsv7142342	copy number variation	1	nstd232	human		GRCh37.p13 chr16: 731,348-731,434 , GRCh38.p12 chr16: 681,348-681,434	STUB1, JMJD8
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
nsv6977619	copy number variation	1	nstd229	human		GRCh38 chr16: 677,793-687,365 , GRCh37.p13 chr16: 727,793-737,365	STUB1-DT, STUB1, 3 more genes
nsv6966485	copy number variation	1	nstd229	human		GRCh38 chr16: 539,563-712,009 , GRCh37.p13 chr16: 589,563-762,009	RHBDL1, PIGQ, 18 more genes
nsv6964587	copy number variation	1	nstd229	human		GRCh38 chr16: 681,201-683,000 , GRCh37.p13 chr16: 731,201-733,000	STUB1, JMJD8, 1 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
nsv6309820	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 729,946-730,042 , GRCh38 chr16: 679,946-680,042	STUB1, STUB1-DT, 1 more genes
nsv6206564	copy number variation	1	nstd214	human		GRCh38 chr16: 679,924-679,988 , GRCh37.p13 chr16: 729,924-729,988	STUB1, JMJD8, 1 more genes
nsv6206174	copy number variation	1	nstd214	human		GRCh38 chr16: 679,958-680,022 , GRCh37.p13 chr16: 729,958-730,022	STUB1, JMJD8, 1 more genes
nsv6202573	copy number variation	1	nstd214	human		GRCh38 chr16: 679,866-679,923 , GRCh37.p13 chr16: 729,866-729,923	STUB1, JMJD8, 1 more genes
nsv6196710	copy number variation	1	nstd214	human		GRCh38 chr16: 679,945-680,041 , GRCh37.p13 chr16: 729,945-730,041	STUB1, JMJD8, 1 more genes
nsv6137723	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 729,959-730,023 , GRCh38 chr16: 679,959-680,023	JMJD8, STUB1, 1 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 507

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Number of Variants: 20

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