foxi3[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
nsv3918504	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr2: 88,421,181-88,553,792 , GRCh37.p13 chr2: 88,640,066-88,772,677 , GRCh38.p12 chr2: 88,340,547-88,473,159	FOXI3, MRPL45P1, 3 more genes
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	FOXI3, DAZAP2P1, 2991 more genes
nsv6634330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419	FOXI3, CYP1B1-AS1, 1649 more genes
nsv3877742	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 74,365,484-89,129,064 , GRCh38.p12 chr2: 74,138,357-88,829,551	FOXI3, RNU6-561P, 253 more genes
nsv3886532	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 74,527,522-89,125,488 , GRCh38.p12 chr2: 74,300,395-88,825,975	FOXI3, RNU6-561P, 249 more genes
nsv3899461	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 85,014,686-88,826,619 , GRCh37 chr2: 85,241,809-89,126,132 , NCBI36 chr2: 85,095,320-88,907,247	FOXI3, CD8A, 115 more genes
nsv6112673	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 88,007,281-90,260,248 , GRCh38.p12 chr2: 87,707,762-90,221,382	FOXI3, IGKV3-20, 122 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	FOXI3, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	FOXI3, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	FOXI3, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	FOXI3, MTND2P22, 3724 more genes
nsv3897079	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 77,025,216-90,282,666 , NCBI36 chr2: 77,105,850-90,982,989 , GRCh37 chr2: 77,252,342-91,619,262	FOXI3, IGKV2D-18, 280 more genes
nsv6314726	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196	FOXI3, ACTG2, 1713 more genes
nsv3878708	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr2: 88,268,212-88,842,463 , GRCh38.p12 chr2: 87,968,693-88,542,945	FOXI3, SPMIP9, 19 more genes
nsv3879104	copy number variation	1	nstd102	human	conflicting data from submitters	GRCh37 chr2: 88,046,608-89,129,064 , GRCh38.p12 chr2: 87,747,089-88,829,551	FOXI3, SMYD1, 31 more genes
nsv3878756	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 88,046,608-89,126,291 , GRCh38.p12 chr2: 87,747,089-88,826,778	FOXI3, NDUFB4P7, 31 more genes
nsv6636373	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 88,046,609-89,126,291 , GRCh38.p12 chr2: 87,747,090-88,826,778	FOXI3, THNSL2, 31 more genes
nsv3887199	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 88,180,842-89,126,291 , GRCh38.p12 chr2: 87,881,323-88,826,778	FOXI3, ANAPC1P5, 28 more genes
nsv3903029	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 87,325,301-92,072,301 , NCBI36 chr2: 87,178,812-91,436,028 , GRCh38 chr2: 87,098,178-91,884,275	FOXI3, SLC9B1P2, 158 more genes
nsv3909593	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 87,602,598-91,619,262 , NCBI36 chr2: 87,456,109-90,982,989 , GRCh38 chr2: 87,375,475-90,282,666	FOXI3, LOC101928371, 130 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 21

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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