foxd4[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
nsv3899067	copy number variation	2	nstd102	human	Benign/Likely benign, Benign	GRCh37 chr9: 118,241-166,977 , GRCh38.p12 chr9: 118,241-166,977	FOXD4, LOC105375942, 1 more genes
nsv3918617	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 101,216-14,640,760 , GRCh38 chr9: 111,216-14,650,762 , GRCh37 chr9: 111,216-14,650,760	FOXD4, TPD52L3, 154 more genes
nsv3895987	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 46,587-13,708,607 , GRCh38.p12 chr9: 46,587-13,708,608	FOXD4, RPL35AP20, 146 more genes
nsv3903094	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 46,587-12,532,584 , GRCh38.p12 chr9: 46,587-12,532,584	FOXD4, RFX3-DT, 136 more genes
nsv3894999	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 13,997-11,376,705 , GRCh38.p12 chr9: 13,997-11,376,705	FOXD4, DMAC1, 136 more genes
nsv3912384	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,993-9,894,905 , GRCh37.p13 chr9: 12,993-9,904,905 , GRCh38.p12 chr9: 12,993-9,904,905	FOXD4, LOC105375951, 131 more genes
nsv3899442	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 46,587-5,486,856 , GRCh38.p12 chr9: 46,587-5,486,856	FOXD4, KANK1, 87 more genes
nsv3916544	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,934-2,780,382 , GRCh37.p13 chr9: 12,934-2,790,382 , GRCh38.p12 chr9: 12,934-2,790,382	FOXD4, H3P29, 44 more genes
nsv4684191	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 1-190,938 , GRCh37.p13 chr9: 10,001-190,938	FOXD4, WASHC1, 10 more genes
nsv3912247	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981	FOXD4, ALOX15P2, 2184 more genes
nsv3890420	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,122,247 , GRCh38.p12 chr9: 10,590-138,231,797	FOXD4, TBC1D13, 2183 more genes
nsv3905118	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,114,095 , GRCh38.p12 chr9: 10,590-138,223,645	FOXD4, MIR219A2, 2183 more genes
nsv3891842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,107,672 , GRCh38.p12 chr9: 10,590-138,217,222	FOXD4, OR13C1P, 2183 more genes
nsv3895453	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 46,587-141,066,491 , GRCh38.p12 chr9: 46,587-138,172,039	FOXD4, RPL19P15, 2176 more genes
nsv3907479	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 62,525-141,006,407 , GRCh38.p12 chr9: 62,525-138,111,955	FOXD4, OR2AM1P, 2174 more genes
nsv3915734	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 13,997-71,015,981 , NCBI36 chr9: 3,997-70,205,801 , GRCh38 chr9: 13,997-68,401,065	FOXD4, CHCHD4P3, 866 more genes
nsv3907430	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 13,997-70,919,878 , GRCh38.p12 chr9: 13,997-68,304,962	FOXD4, LOC105379448, 861 more genes
nsv3921759	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,934-65,222,364 , GRCh37.p13 chr9: 12,934-65,482,544 , GRCh38.p12 chr9: 12,934-66,233,120	FOXD4, SPATA31A6, 824 more genes
nsv3897423	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 32,396-39,140,211 , GRCh38.p12 chr9: 32,396-39,140,214	FOXD4, LOC105375985, 583 more genes
nsv3896247	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 46,587-22,012,051 , GRCh38.p12 chr9: 46,587-22,012,052	FOXD4, DOCK8-AS2, 273 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