tbx3[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 12

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv997201	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr12: 114,670,254-114,684,164 , GRCh37 chr12: 115,108,059-115,121,969	TBX3, TBX3-AS1
nsv3907306	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 115,147,769-115,250,436 , GRCh38.p12 chr12: 114,709,964-114,812,631	LOC105369999, TBX3-AS1
nsv1398091	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 115,109,877-115,120,812 , GRCh38.p12 chr12: 114,672,072-114,683,007	TBX3, TBX3-AS1
nsv3890891	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 114,995,645-115,376,925 , GRCh38.p12 chr12: 114,557,840-114,939,120	TBX3, OSTF1P1, 2 more genes
nsv3898489	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 114,948,986-115,167,687 , GRCh38.p12 chr12: 114,511,181-114,729,882	TBX3, OSTF1P1, 1 more genes
nsv6309391	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 113,120,652-115,362,584 , GRCh38.p12 chr12: 112,682,847-114,924,779	TBX3, LOC105369993, 41 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	TBX3, RNA5SP369, 2454 more genes
nsv3905447	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316	TBX3, LOH12CR2, 2452 more genes
nsv3897722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059	TBX3, RNU4ATAC16P, 2452 more genes
nsv3914194	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807	TBX3, BTG1P1, 2451 more genes
nsv3904719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532	TBX3, OR5BT1P, 2441 more genes
nsv3913894	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 113,190,591-132,287,975 , GRCh38 chr12: 114,268,403-133,201,316 , GRCh37 chr12: 114,706,208-133,777,902	TBX3, TAOK3, 386 more genes

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