dbVar for Gene (Select 57585) - 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
nsv7098880	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 811,896-2,130,379 , GRCh38.p12 chr16: 761,896-2,080,378	TPSP1, NPW, 78 more genes
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
nsv7073654	inversion	1	nstd229	human		GRCh38 chr16: 840,992-1,785,906 , GRCh37.p13 chr16: 890,992-1,835,907	UBE2I, CRAMP1, 45 more genes
nsv7064563	inversion	1	nstd229	human		GRCh38 chr16: 1,279,128-1,693,078 , GRCh37.p13 chr16: 1,329,129-1,743,079	UNKL, CRAMP1, 20 more genes
nsv6977654	copy number variation	1	nstd229	human		GRCh38 chr16: 1,592,232-1,728,113 , GRCh37.p13 chr16: 1,642,233-1,778,114	MAPK8IP3-AS1, JPT2, 4 more genes
nsv6977365	copy number variation	1	nstd229	human		GRCh38 chr16: 1,639,387-1,639,420 , GRCh37.p13 chr16: 1,689,388-1,689,421	CRAMP1
nsv6975574	copy number variation	1	nstd229	human		GRCh38 chr16: 1,635,031-1,635,165 , GRCh37.p13 chr16: 1,685,032-1,685,166	CRAMP1
nsv6973645	copy number variation	1	nstd229	human		GRCh38 chr16: 1,642,663-1,650,178 , GRCh37.p13 chr16: 1,692,664-1,700,179	CRAMP1
nsv6969260	copy number variation	1	nstd229	human		GRCh38 chr16: 1,647,327-1,650,368 , GRCh37.p13 chr16: 1,697,328-1,700,369	CRAMP1
nsv6965261	copy number variation	1	nstd229	human		GRCh38 chr16: 1,351,958-1,810,245 , GRCh37.p13 chr16: 1,401,959-1,860,246	JPT2, UNKL, 26 more genes
nsv6964153	copy number variation	1	nstd229	human		GRCh38 chr16: 1,677,110-1,678,823 , GRCh37.p13 chr16: 1,727,111-1,728,824	CRAMP1, JPT2
nsv6962303	copy number variation	1	nstd229	human		GRCh38 chr16: 1,118,142-1,673,202 , GRCh37.p13 chr16: 1,168,142-1,723,203	TJP1P1, TELO2, 27 more genes
nsv6961828	copy number variation	1	nstd229	human		GRCh38 chr16: 1,397,353-1,610,652 , GRCh37.p13 chr16: 1,447,354-1,660,653	IFT140, CRAMP1, 12 more genes
nsv6960266	copy number variation	1	nstd229	human		GRCh38 chr16: 1,675,563-1,678,811 , GRCh37.p13 chr16: 1,725,564-1,728,812	JPT2, CRAMP1
nsv6959087	copy number variation	1	nstd229	human		GRCh38 chr16: 1,654,605-1,688,965 , GRCh37.p13 chr16: 1,704,606-1,738,966	CRAMP1, JPT2
nsv6958475	copy number variation	1	nstd229	human		GRCh38 chr16: 1,648,600-1,653,077 , GRCh37.p13 chr16: 1,698,601-1,703,078	CRAMP1
nsv6637768	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 1,129,080-2,021,055 , GRCh38.p12 chr16: 1,079,080-1,971,054	CRAMP1, LOC105371046, 57 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

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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

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Items: 1 to 20 of 357

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Number of Variants: 20

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