folr1[All Fields] AND 1[has_clinical] - dbVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 16

loading data ...

Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6309286	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr11: 71,903,218-71,903,405 , GRCh38.p12 chr11: 72,192,174-72,192,361	FOLR1
nsv7093946	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,903,218-72,019,668 , GRCh38.p12 chr11: 72,192,174-72,308,624	FOLR1, PHOX2A, 5 more genes
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	FOLR1, FAUP4, 2031 more genes
nsv3915804	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,680,927-77,943,941 , NCBI36 chr11: 71,358,575-77,621,589 , GRCh38 chr11: 71,969,881-78,232,895	FOLR1, TPBGL, 173 more genes
nsv3916301	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 71,928,796-77,064,521 , GRCh37 chr11: 71,639,842-76,751,808 , NCBI36 chr11: 71,317,490-76,453,216	FOLR1, RN7SL786P, 146 more genes
nsv3919985	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 70,668,528-72,528,680 , GRCh37.p13 chr11: 70,990,880-72,851,032 , GRCh38.p12 chr11: 71,279,834-73,139,987	FOLR1, OR7E128P, 68 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	FOLR1, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	FOLR1, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	FOLR1, IGHMBP2, 2829 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	FOLR1, PYGM, 2125 more genes
nsv3898361	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202	FOLR1, SESN3, 694 more genes
nsv6314007	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 71,567,724-72,488,649 , GRCh38.p12 chr11: 71,856,678-72,777,604	FOLR1, STARD10, 38 more genes
nsv7094183	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 71,146,421-75,283,128 , GRCh38.p12 chr11: 71,435,375-75,572,083	FOLR1, LOC112268078, 142 more genes
nsv3921153	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr11: 71,164,008-72,309,374 , GRCh37 chr11: 71,088,949-72,020,418 , NCBI36 chr11: 70,552,702-71,698,066	FOLR1, LOC220077, 47 more genes
nsv4681893	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 71,146,401-71,907,241 , GRCh38.p12 chr11: 71,435,355-72,196,197	FOLR1, OR7E128P, 39 more genes
nsv6637545	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 71,777,538-72,144,933 , GRCh38.p12 chr11: 72,066,492-72,433,889	FOLR1, CLPB, 15 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

folr1[All Fields] AND 1[has_clinical] (17)
dbVar

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)