tbx18[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 18

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3881356	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 85,147,411-85,397,988 , GRCh38.p12 chr6: 84,437,693-84,688,270	TBX18, LINC01611, 2 more genes
nsv3922692	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 85,277,527-85,774,647 , GRCh38 chr6: 84,511,090-85,008,210 , GRCh37 chr6: 85,220,808-85,717,928	TBX18, TBX18-AS1, 2 more genes
nsv4675560	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 85,220,808-85,517,846 , GRCh38.p12 chr6: 84,511,090-84,808,128	TBX18, TBX18-AS1, 1 more genes
nsv3921478	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 76,692,636-93,477,232 , GRCh38 chr6: 75,926,199-92,710,793 , GRCh37 chr6: 76,635,916-93,420,511	TBX18, SPACA1, 187 more genes
nsv3923528	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 84,604,741-99,376,910 , GRCh38 chr6: 83,838,303-98,822,313 , GRCh37 chr6: 84,548,022-99,270,189	TBX18, RNU4-72P, 157 more genes
nsv3914309	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 82,569,098-93,753,476 , NCBI36 chr6: 83,335,534-94,519,915 , GRCh37 chr6: 83,278,815-94,463,194	TBX18, ME1, 136 more genes
nsv3873582	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 83,319,012-91,907,669 , GRCh38.p12 chr6: 82,609,295-91,197,951	TBX18, LOC105377882, 117 more genes
nsv6290989	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 83,141,523-88,023,466 , GRCh38.p12 chr6: 82,431,806-87,313,748	TBX18, KRT18P30, 58 more genes
nsv7098884	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 82,828,591-86,578,811 , GRCh38.p12 chr6: 82,118,874-85,869,093	TBX18, LOC105377879, 47 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	TBX18, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	TBX18, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	TBX18, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	TBX18, ITPR3, 2905 more genes
nsv3919111	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637	TBX18, RNU6-770P, 810 more genes
nsv6313857	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492	TBX18, LOC101928570, 288 more genes
nsv3872975	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 81,261,418-97,796,269 , GRCh38.p12 chr6: 80,551,701-97,348,393	TBX18, ME1, 178 more genes
nsv6634392	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297	TBX18, MTHFD2P2, 212 more genes
nsv7097097	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 84,765,038-86,267,798 , GRCh38.p12 chr6: 84,055,319-85,558,080	TBX18, MRAP2, 18 more genes

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