mob4[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3884752	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr2: 197,487,026-197,498,868 , GRCh37.p13 chr2: 198,351,750-198,363,592	HSPD1, HSPE1-MOB4, 2 more genes
nsv5381571	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 198,351,760-198,363,582 , GRCh38.p12 chr2: 197,487,036-197,498,858	HSPE1, SNORA105B, 2 more genes
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	MOB4, DAZAP2P1, 2991 more genes
nsv3894939	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 175,471,822-204,514,516 , GRCh37 chr2: 175,763,576-204,806,271 , GRCh38 chr2: 174,898,848-203,941,548	MOB4, TRE-TTC9-1, 412 more genes
nsv6315398	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 185,697,659-213,002,074 , GRCh38.p12 chr2: 184,832,932-212,137,349	MOB4, LOC107985785, 381 more genes
nsv3899404	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 176,877,419-202,612,758 , GRCh37 chr2: 177,169,173-202,904,513 , GRCh38 chr2: 176,304,445-202,039,790	MOB4, LINC01877, 326 more genes
nsv3896612	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 192,938,826-215,705,052 , NCBI36 chr2: 193,511,797-216,278,020 , GRCh37 chr2: 193,803,552-216,569,775	MOB4, MTND4P30, 320 more genes
nsv3895293	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 178,738,797-199,390,216 , NCBI36 chr2: 178,447,043-199,098,461 , GRCh38 chr2: 177,874,070-198,525,492	MOB4, CALCRL-AS1, 218 more genes
nsv6637127	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 189,909,904-209,468,383 , GRCh38.p12 chr2: 189,045,178-208,603,658	MOB4, LOC100421409, 310 more genes
nsv3891560	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 186,027,472-201,059,372 , NCBI36 chr2: 186,600,444-201,632,340 , GRCh37 chr2: 186,892,199-201,924,095	MOB4, AOX1, 174 more genes
nsv6636571	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 187,152,754-199,960,525 , GRCh38.p12 chr2: 186,288,027-199,095,802	MOB4, GAPDHP59, 135 more genes
nsv3884561	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 189,490,490-200,615,496 , GRCh38.p12 chr2: 188,625,763-199,750,773	MOB4, C2orf88, 120 more genes
nsv3884912	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 191,750,202-202,297,376 , GRCh38.p12 chr2: 190,885,476-201,432,653	MOB4, CLK1, 134 more genes
nsv4716529	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 190,345,272-200,212,289 , GRCh38.p12 chr2: 189,480,546-199,347,566	MOB4, C2orf66, 105 more genes
nsv3881119	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 193,537,927-202,027,736 , GRCh38.p12 chr2: 192,673,201-201,163,013	MOB4, LOC105376755, 107 more genes
nsv3908231	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 196,233,563-204,542,456 , GRCh38 chr2: 195,660,594-203,969,488 , GRCh37 chr2: 196,525,318-204,834,211	MOB4, LINC01877, 170 more genes
nsv3876959	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 194,581,315-201,752,422 , GRCh38.p12 chr2: 193,716,591-200,887,699	MOB4, LOC101927741, 87 more genes
nsv4453090	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 195,786,723-200,531,127 , GRCh38.p12 chr2: 194,921,999-199,666,404	MOB4, RFTN2, 54 more genes
nsv3875157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 196,581,377-200,947,041 , GRCh38.p12 chr2: 195,716,653-200,082,318	MOB4, C2orf66, 53 more genes
nsv3907002	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 195,379,883-199,410,661 , GRCh38 chr2: 194,515,159-198,545,937 , NCBI36 chr2: 195,088,128-199,118,906	MOB4, LOC105373817, 47 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:

Search results

Items: 1 to 20 of 44

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

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

Search results

Items: 1 to 20 of 44

Page of 3

Number of Variants: 20

Page of 3

Supplemental Content

Find related data

Search details

Recent activity