pitx2[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
nsv4682761	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 111,539,261-111,554,174 , GRCh38.p12 chr4: 110,618,105-110,633,018	PITX2
nsv6311706	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 111,539,281-111,554,154 , GRCh38.p12 chr4: 110,618,125-110,632,998	PITX2
nsv3883090	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 111,539,205-111,543,628 , GRCh38 chr4: 110,618,049-110,622,472	PITX2
nsv997231	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr4: 110,617,423-110,642,123 , GRCh37 chr4: 111,538,579-111,563,279	PITX2
nsv5673644	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 111,539,261-111,543,636 , GRCh38.p12 chr4: 110,618,105-110,622,480	PITX2
nsv3872588	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 111,539,337-111,542,501 , GRCh38 chr4: 110,618,181-110,621,345	PITX2
nsv3883978	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 111,540,657-111,544,304 , GRCh38.p12 chr4: 110,619,501-110,623,148	PITX2
nsv3875262	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 111,396,948-111,664,814 , GRCh38.p12 chr4: 110,475,792-110,743,658	PITX2, LOC105377363, 2 more genes
nsv3879891	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 111,426,357-111,990,971 , GRCh38.p12 chr4: 110,505,201-111,069,815	PITX2, ENPEP, 5 more genes
nsv4729714	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 111,334,313-113,223,858 , GRCh38.p12 chr4: 110,413,157-112,302,702	PITX2, PANCR, 20 more genes
nsv3873978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724	PITX2, LOC100422029, 2358 more genes
nsv3876533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611	PITX2, LOC100420289, 2347 more genes
nsv3884499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286	PITX2, MTND4LP29, 2341 more genes
nsv3880085	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318	PITX2, LOC112268460, 2345 more genes
nsv3883791	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495	PITX2, LOC105377343, 2341 more genes
nsv3875534	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 93,071,152-190,957,473 , GRCh38.p12 chr4: 92,150,001-190,036,318	PITX2, KLKB1, 1118 more genes
nsv6291432	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354	PITX2, SNHG27, 1091 more genes
nsv3874596	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 109,199,664-189,752,726 , GRCh38.p12 chr4: 108,278,508-188,831,572	PITX2, RPL6P12, 938 more genes
nsv6313878	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 104,715,235-145,252,595 , GRCh38.p12 chr4: 103,794,078-144,331,443	PITX2, LINC00613, 448 more genes
nsv3920388	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 97,014,044-137,331,362 , NCBI36 chr4: 97,233,067-137,550,812 , GRCh38 chr4: 96,092,893-136,410,207	PITX2, MIR576, 447 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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