foxb2[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3897053	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 68,999,534-84,656,998 , GRCh38.p12 chr9: 40,926,305-82,042,083	FOXB2, PABIR1, 397 more genes
nsv3893036	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 68,838,523-83,340,723 , GRCh38.p12 chr9: 40,915,719-80,725,808	FOXB2, RPL35AP21, 379 more genes
nsv3915174	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 70,304,266-85,474,962 , GRCh38 chr9: 68,499,530-83,670,227 , GRCh37 chr9: 71,130,848-86,285,142	FOXB2, LOC107987086, 183 more genes
nsv4455928	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 70,974,661-81,829,792 , GRCh38.p12 chr9: 68,359,745-79,214,877	FOXB2, RPL35AP21, 134 more genes
nsv3904790	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 74,534,790-84,014,155 , GRCh38.p12 chr9: 71,919,874-81,399,240	FOXB2, LOC105376099, 108 more genes
nsv3913411	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 75,511,422-82,175,364 , GRCh37 chr9: 76,321,602-82,985,544 , GRCh38 chr9: 73,706,686-80,370,629	FOXB2, OTX2P1, 72 more genes
nsv3923526	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 74,029,084-79,136,863 , GRCh37 chr9: 74,839,264-79,947,043 , GRCh38 chr9: 72,224,348-77,332,127	FOXB2, GCNT1, 65 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	FOXB2, 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	FOXB2, 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	FOXB2, 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	FOXB2, 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	FOXB2, RPL19P15, 2176 more genes
nsv3900967	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 163,131-141,122,114 , GRCh38.p12 chr9: 163,131-138,231,664	FOXB2, BANCR, 2173 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	FOXB2, OR2AM1P, 2174 more genes
nsv3922684	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897	FOXB2, TDRD7, 2170 more genes
nsv3919257	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 204,193-141,073,897 , GRCh38 chr9: 204,193-138,179,445 , NCBI36 chr9: 194,193-140,193,718	FOXB2, LOC107987031, 2169 more genes
nsv3915973	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr9: 193,412-138,159,073 , GRCh37 chr9: 68,420,641-141,053,525 , NCBI36 chr9: 67,910,461-140,173,346	FOXB2, CTNNAL1, 2170 more genes
nsv3911025	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 193,412-138,124,524 , NCBI36 chr9: 194,090-140,138,797 , GRCh37 chr9: 204,090-141,018,976	FOXB2, RORB-AS1, 2168 more genes
nsv3921598	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389	FOXB2, PGAP4, 2167 more genes
nsv4457273	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936	FOXB2, CDRT15P14, 2167 more genes

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Number of Variants: 20

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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 43

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Number of Variants: 20

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