dbVar for Gene (Select 106478991) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5672807	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 92,002,837-103,343,314 , GRCh38.p12 chr13: 91,350,583-102,690,964	RPL7L1P12, MIR548AS, 153 more genes
nsv5672796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 94,679,977-111,536,145 , GRCh38.p12 chr13: 94,027,723-110,883,798	LINC00359, LOC107984609, 220 more genes
nsv5564510	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053	RN7SL272P, DIAPH3, 1333 more genes
nsv5033445	inversion	1	nstd200	human		GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658	, RPL15P18, 564 more genes
nsv4871044	inversion	1	nstd200	human		GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344	, TUBGCP3, 564 more genes
nsv4683528	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 100,038,233-100,638,902 , GRCh38.p12 chr13: 99,385,979-99,986,648	CLYBL-AS2, RNY3P6, 14 more genes
nsv4675892	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 96,240,346-106,103,782 , GRCh38.p12 chr13: 95,588,092-105,451,433	LOC105370328, LINC00554, 132 more genes
nsv4675850	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258	TEX30, LOC101927712, 680 more genes
nsv4675644	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 96,895,656-115,107,733 , GRCh38.p12 chr13: 96,243,402-114,342,258	ZIC2, LINC03032, 266 more genes
nsv4456561	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 61,775,567-115,107,733 , GRCh38.p12 chr13: 61,201,433-114,342,258	LOC105370262, LINC01080, 609 more genes
nsv4456260	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 94,849,303-115,107,733 , GRCh38.p12 chr13: 94,197,049-114,342,258	F10, FKSG29, 300 more genes
nsv4431864	copy number variation	1	nstd172	human		GRCh38.p12 chr13: 99,499,639-99,500,642 , GRCh37.p13 chr13: 100,151,893-100,152,896	TM9SF2, LINC01232, 1 more genes
nsv4223645	copy number variation	1	nstd166	human		GRCh37.p13 chr13: 100,149,000-100,154,000 , GRCh38.p12 chr13: 99,496,746-99,501,746	LINC01232, LINC00449, 1 more genes
nsv3924676	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 18,456,040-114,340,285 , GRCh37 chr13: 19,030,180-115,105,760 , NCBI36 chr13: 17,928,180-114,123,862	GRTP1, FABP5P1, 1334 more genes
nsv3924528	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908	LOC105370271, OR7E33P, 925 more genes
nsv3923796	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 78,471,454-114,110,683 , GRCh38 chr13: 78,999,318-114,327,106 , GRCh37 chr13: 79,573,453-115,085,141	LOC107984608, TEX29, 423 more genes
nsv3923642	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 44,738,887-115,085,141 , NCBI36 chr13: 43,636,887-114,110,750 , GRCh38 chr13: 44,164,751-114,327,173	LOC107984554, HNRNPA1P18, 861 more genes
nsv3922463	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 18,418,322-114,088,205 , GRCh37 chr13: 19,520,322-115,070,103 , GRCh38 chr13: 18,946,182-114,304,628	TULP3P1, LOC105370349, 1311 more genes
nsv3922317	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 95,744,855-110,863,818 , GRCh37 chr13: 96,397,109-111,516,165 , NCBI36 chr13: 95,195,110-110,314,166	RN7SKP9, ARF4P3, 188 more genes
nsv3921223	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 19,671,934-114,340,331 , NCBI36 chr13: 19,144,074-114,123,908 , GRCh37 chr13: 20,246,074-115,085,141	TRIM60P13, LINC00351, 1289 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 151

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 151

Page of 8

Number of Variants: 20

Page of 8

Supplemental Content

Find related data

Recent activity