dbVar for Gene (Select 100129727) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6112714	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481	RNU6-789P, FAM86HP, 169 more genes
nsv6112709	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 123,000,000-129,700,000 , GRCh38.p12 chr3: 123,281,153-129,981,157	OR7E97P, MARK3P3, 160 more genes
nsv6112688	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144	RNU4-62P, MTCO1P29, 169 more genes
nsv6112686	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 127,889,037-128,565,901 , GRCh38.p12 chr3: 128,170,194-128,847,058	EEFSEC, MARK2P8, 16 more genes
nsv5316764	copy number variation	1	nstd204	human		GRCh38.p13 chr3: 128,515,182-128,985,140 , GRCh37.p13 chr3: 128,234,025-128,703,983	CFAP92, FTH1P4, 14 more genes
nsv5239966	copy number variation	1	nstd204	human		GRCh38.p13 chr3: 128,514,477-128,539,072 , GRCh37.p13 chr3: 128,233,320-128,257,915	TMED10P2
nsv5231169	copy number variation	1	nstd204	human		GRCh38.p13 chr3: 128,514,801-128,660,200 , GRCh37.p13 chr3: 128,233,644-128,379,043	RPN1, LINC01565, 1 more genes
nsv5036857	inversion	1	nstd200	human		GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646	, FBRSL1P1, 801 more genes
nsv4914736	copy number variation	1	nstd200	human		GRCh38 chr3: 128,515,192-128,985,136 , GRCh37.p13 chr3: 128,234,035-128,703,979	POU5F1P6, ACAD9, 14 more genes
nsv4794338	copy number variation	1	nstd200	human		GRCh37 chr3: 128,234,035-128,703,979 , GRCh38.p12 chr3: 128,515,192-128,985,136	RAB7A, MARK3P3, 14 more genes
nsv4682915	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 128,199,842-128,631,470 , GRCh38.p12 chr3: 128,480,999-128,912,627	MARK2P6, GATA2-AS1, 17 more genes
nsv4327395	inversion	1	nstd166	human		GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842	, ACTG1P1, 1039 more genes
nsv4326687	inversion	1	nstd166	human		GRCh37.p13 chr3: 127,535,894-128,720,376 , GRCh38.p12 chr3: 127,817,051-129,001,533	RAB7A, MGLL, 32 more genes
nsv3923961	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 126,797,420-128,946,623 , GRCh37 chr3: 126,516,263-128,665,466 , NCBI36 chr3: 127,998,953-130,148,156	RUVBL1-AS1, LOC105374096, 49 more genes
nsv3922717	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168	OR7E53P, HSPA8P9, 794 more genes
nsv3920834	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 127,308,312-142,119,621 , GRCh38 chr3: 126,106,779-140,918,089 , GRCh37 chr3: 125,825,622-140,636,931	NCK1-DT, LOC107986126, 271 more genes
nsv3918981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446	LINC02614, LINC02054, 1469 more genes
nsv3918094	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 113,822,514-129,935,667 , GRCh38 chr3: 112,620,977-128,734,134 , GRCh37 chr3: 112,339,824-128,452,977	QTRT2, MIR544B, 284 more genes
nsv3912335	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr3: 128,809,478-134,768,195 , GRCh37 chr3: 127,326,788-133,285,505 , GRCh38 chr3: 127,607,945-133,566,661	ACP3, FTH1P4, 130 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	NDUFB4, LOC105374108, 2876 more genes

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

Send to:

Links from Gene

Items: 1 to 20 of 92

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Recent activity

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 92

Page of 5

Number of Variants: 20

Page of 5

Supplemental Content

Find related data

Recent activity