cfl2[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
nsv4453660	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 34,710,372-34,713,686 , GRCh37 chr14: 35,179,578-35,182,892	CFL2
nsv3885635	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr14: 35,182,051-35,183,766 , GRCh38 chr14: 34,712,845-34,714,560	CFL2
nsv4683923	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 35,179,578-35,182,892 , GRCh38.p12 chr14: 34,710,372-34,713,686	CFL2
nsv4455836	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 35,150,795-35,252,969 , GRCh38.p12 chr14: 34,681,589-34,783,763	CFL2, RPL23AP8, 3 more genes
nsv6314715	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884	CFL2, HNRNPC, 616 more genes
nsv3916277	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 19,734,944-44,823,755 , GRCh38 chr14: 20,196,945-45,284,802 , GRCh37 chr14: 20,665,104-45,754,005	CFL2, MIR208B, 600 more genes
nsv3917157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 24,018,169-42,452,605 , GRCh38 chr14: 23,548,960-41,983,402 , NCBI36 chr14: 23,088,009-41,522,355	CFL2, LINC02300, 274 more genes
nsv3916173	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 33,118,898-48,418,573 , GRCh37.p13 chr14: 34,049,147-49,348,823 , GRCh38.p12 chr14: 33,579,941-48,879,620	CFL2, TTC6, 178 more genes
nsv3924751	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 31,261,477-45,154,334 , GRCh38 chr14: 30,792,271-44,685,131 , NCBI36 chr14: 30,331,228-44,224,084	CFL2, DNAJC8P1, 171 more genes
nsv5381757	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 33,608,925-44,570,367 , GRCh38.p12 chr14: 33,139,719-44,101,164	CFL2, RPLP0P3, 131 more genes
nsv3912278	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 33,880,412-42,359,485 , NCBI36 chr14: 33,419,369-41,898,438 , GRCh37 chr14: 34,349,618-42,828,688	CFL2, RPL23AP8, 120 more genes
nsv3922917	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 30,851,760-38,181,546 , NCBI36 chr14: 29,921,511-37,251,297 , GRCh38 chr14: 30,382,554-37,712,341	CFL2, MBIP, 124 more genes
nsv7093397	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 34,904,407-36,784,136 , GRCh38.p12 chr14: 34,435,201-36,314,930	CFL2, DPRXP3, 51 more genes
nsv3902883	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863	CFL2, LOC440181, 1998 more genes
nsv3907460	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456	CFL2, BANF1P1, 1996 more genes
nsv3899639	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456	CFL2, LOC100289511, 1996 more genes
nsv3903256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050	CFL2, DHRS7, 1946 more genes
nsv3919106	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482	CFL2, SRMP2, 1929 more genes
nsv3904265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229	CFL2, CRIP1, 1929 more genes
nsv3917422	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478	CFL2, MIR656, 1918 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 32

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 32

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity