alb[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
nsv3898370	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 73,915,803-73,922,221 , GRCh38.p12 chr17: 75,919,722-75,926,140	FBF1
nsv3908048	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr17: 73,929,152-73,955,205 , GRCh38.p12 chr17: 75,933,071-75,959,124	ACOX1, FBF1
nsv4769393	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 73,926,095-73,949,575 , GRCh38.p12 chr17: 75,930,014-75,953,494	FBF1, ACOX1
nsv3897135	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 73,872,539-73,922,221 , GRCh38.p12 chr17: 75,876,458-75,926,140	FBF1, MRPL38, 2 more genes
nsv3894017	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 73,872,948-73,922,221 , GRCh38.p12 chr17: 75,876,867-75,926,140	TRIM47, FBF1, 2 more genes
nsv3895893	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 73,886,097-73,914,116 , GRCh38.p12 chr17: 75,890,016-75,918,035	FBF1, TRIM65, 1 more genes
nsv3911811	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577	PRPSAP1, CACNG1, 1350 more genes
nsv3923759	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 58,862,002-102,129,682 , GRCh37.p13 chr4: 59,167,245-101,910,659 , GRCh38.p12 chr4: 58,301,079-100,989,502	ALB, EREG, 530 more genes
nsv5674237	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872	ALB, FTLP10, 335 more genes
nsv4729598	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 71,412,409-87,920,784 , GRCh38.p12 chr4: 70,546,692-86,999,632	ALB, PTPN11P5, 244 more genes
nsv6314916	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 67,833,055-82,716,065 , GRCh37.p13 chr4: 68,698,773-83,637,218	ALB, MICOS10P4, 274 more genes
nsv4674589	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 72,680,879-86,426,232 , GRCh38.p12 chr4: 71,815,162-85,505,079	ALB, SOWAHB, 211 more genes
nsv6313740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 61,867,555-74,711,517 , GRCh38.p12 chr4: 61,001,837-73,845,800	ALB, CXCL8, 175 more genes
nsv4674141	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,950,363-79,738,598 , GRCh38.p12 chr4: 68,084,645-78,817,444	ALB, COX18, 216 more genes
nsv3884502	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 66,017,575-76,772,947 , GRCh38.p12 chr4: 65,151,857-75,851,794	ALB, RNU2-40P, 188 more genes
nsv6313715	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 73,055,313-80,083,154 , GRCh38.p12 chr4: 72,189,596-79,162,000	ALB, CCNG2, 129 more genes
nsv4456138	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 71,561,780-78,304,341 , GRCh38.p12 chr4: 70,696,063-77,383,187	ALB, ANKRD17-DT, 119 more genes
nsv3919795	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 71,144,026-71,478,420 , GRCh37 chr17: 73,632,431-73,966,825 , GRCh38 chr17: 75,636,351-75,970,744	ITGB4, TRIM65, 15 more genes
nsv3873978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724	ALB, LOC100422029, 2358 more genes
nsv3876533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611	ALB, LOC100420289, 2347 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 52

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 52

Page of 3

Number of Variants: 20

Page of 3

Supplemental Content

Find related data

Search details

Recent activity