fras1[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
nsv4456615	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 79,214,098-79,261,919 , GRCh38.p12 chr4: 78,292,944-78,340,765	FRAS1
nsv4450676	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 78,499,721-78,526,657 , GRCh37 chr4: 79,420,875-79,447,811	FRAS1
nsv7098981	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 79,362,452-79,367,880 , GRCh38.p12 chr4: 78,441,298-78,446,726	FRAS1
nsv4674755	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 79,112,309-79,175,262 , GRCh38.p12 chr4: 78,191,155-78,254,108	FRAS1
nsv7096868	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 78,979,164-78,979,259 , GRCh38.p12 chr4: 78,058,010-78,058,105	FRAS1
nsv6289835	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 79,189,825-79,219,911 , GRCh38.p12 chr4: 78,268,671-78,298,757	FRAS1, SNORD161
nsv3912544	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 79,450,270-79,681,469 , GRCh37.p13 chr4: 79,231,246-79,462,445 , GRCh38.p12 chr4: 78,310,092-78,541,291	FRAS1, MICOS10P4
nsv4457070	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 79,097,584-79,166,086 , GRCh38.p12 chr4: 78,176,430-78,244,932	FRAS1, SERBP1P5
nsv6314463	complex chromosomal rearrangement	2	nstd102	human	Uncertain significance	GRCh38.p12 chr4: 78,310,322-78,310,322 , GRCh38.p12 chr4: 78,310,337-78,310,337 , GRCh37 chr4: 79,231,476-79,231,476 , GRCh37 chr4: 79,231,491-79,231,491 , GRCh37 chr3: 161,887,906-161,887,906 , GRCh37 chr3: 161,887,919-161,887,919 , GRCh38.p12 chr3: 162,170,118-162,170,118 , GRCh38.p12 chr3: 162,170,131-162,170,131	FRAS1, LOC107986048
nsv6636341	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 78,947,327-79,326,031 , GRCh38.p12 chr4: 78,026,173-78,404,877	FRAS1, SERBP1P5, 3 more genes
nsv3923458	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 79,281,132-79,698,720 , GRCh37.p13 chr4: 79,062,108-79,479,696 , GRCh38.p12 chr4: 78,140,954-78,558,542	FRAS1, SNORD161, 3 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	FRAS1, EREG, 530 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	FRAS1, 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	FRAS1, 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	FRAS1, SOWAHB, 211 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	FRAS1, COX18, 216 more genes
nsv3922666	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 76,597,345-85,234,472 , GRCh38 chr4: 75,453,111-84,094,295 , GRCh37 chr4: 76,378,321-85,015,448	FRAS1, LOC100421142, 146 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	FRAS1, CCNG2, 129 more genes
nsv4457234	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 78,769,297-84,968,832 , GRCh38.p12 chr4: 77,848,143-84,047,679	FRAS1, OR7E94P, 87 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	FRAS1, LOC100422029, 2358 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 37

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 37

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity