tbx2[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
nsv3908170	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 59,486,799-59,490,235 , GRCh38.p12 chr17: 61,409,438-61,412,874	TBX2, LINC02875
nsv3895539	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 59,479,113-59,490,235 , GRCh38.p12 chr17: 61,401,752-61,412,874	TBX2, LINC02875
nsv3892999	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 59,482,968-59,490,235 , GRCh38.p12 chr17: 61,405,607-61,412,874	TBX2, LINC02875
nsv3891693	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 59,482,968-59,489,787 , GRCh38.p12 chr17: 61,405,607-61,412,426	TBX2, LINC02875
nsv3901228	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr17: 59,419,931-59,500,353 , GRCh38.p12 chr17: 61,342,570-61,422,992	TBX2, LOC101927855, 3 more genes
nsv3909044	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 59,470,597-59,489,787 , GRCh38.p12 chr17: 61,393,236-61,412,426	TBX2, TBX2-AS1, 2 more genes
nsv3920641	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr17: 61,331,901-61,424,019 , GRCh37 chr17: 59,409,262-59,501,380 , NCBI36 chr17: 56,764,044-56,856,162	TBX2, LOC101927855, 3 more genes
nsv3911811	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577	TBX2, PRPSAP1, 1350 more genes
nsv3895056	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 56,623,275-60,285,107 , GRCh38.p12 chr17: 58,545,914-62,207,746	TBX2, MIR454, 87 more genes
nsv3918670	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 58,172,700-60,315,303 , GRCh38 chr17: 60,095,339-62,237,942 , NCBI36 chr17: 55,527,482-57,670,085	TBX2, MED13, 37 more genes
nsv3916375	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 55,475,591-57,580,872 , GRCh38 chr17: 60,043,448-62,148,729 , GRCh37 chr17: 58,120,809-60,226,090	TBX2, HEATR6-DT, 41 more genes
nsv3911620	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 58,332,553-60,315,303 , GRCh38 chr17: 60,255,192-62,237,942 , NCBI36 chr17: 55,687,335-57,670,085	TBX2, INTS2, 31 more genes
nsv3901406	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 58,934,659-60,395,826 , NCBI36 chr17: 56,289,441-57,750,608 , GRCh38.p12 chr17: 60,857,298-62,318,465	TBX2, INTS2, 18 more genes
nsv3318990	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chr17: 58,113,002-60,275,809 , GRCh38.p12 chr17: 60,035,641-62,198,448	TBX2, CA4, 41 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	TBX2, MIR3185, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	TBX2, P4HB, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	TBX2, MIR21, 2366 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	TBX2, SMURF2, 2366 more genes
nsv3914783	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577	TBX2, LOC105371922, 1855 more genes
nsv3909511	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846	TBX2, FOXK2, 958 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 32

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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