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

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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
nsv3924180	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 65,316,269-84,193,229 , GRCh38 chr6: 64,549,655-83,426,791 , GRCh37 chr6: 65,259,548-84,136,510	TPBG, LOC105377875, 188 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	TPBG, SPACA1, 187 more genes
nsv3889959	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 73,674,612-84,829,774 , GRCh38.p12 chr6: 72,964,889-84,120,055	TPBG, MRAP2, 125 more genes
nsv6291322	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 72,799,054-83,275,894 , GRCh38.p12 chr6: 72,089,351-82,566,177	TPBG, RPS27P15, 118 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	TPBG, LOC105377879, 47 more genes
nsv1398415	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 83,013,454-84,395,825 , GRCh38.p12 chr6: 82,303,737-83,686,106	TPBG, PGM3, 10 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	TPBG, 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	TPBG, 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	TPBG, 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	TPBG, 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	TPBG, 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	TPBG, 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	TPBG, ME1, 178 more genes
nsv3911622	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr6: 79,678,455-84,862,865 , GRCh37.p13 chr6: 79,621,736-84,806,146 , GRCh38.p12 chr6: 78,912,019-84,096,427	TPBG, BCKDHB, 55 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	TPBG, MTHFD2P2, 212 more genes
nsv4675056	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 82,620,262-84,201,117 , GRCh38.p12 chr6: 81,910,545-83,491,398	TPBG, LOC100132659, 14 more genes
nsv4455848	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 82,987,696-84,007,694 , GRCh38.p12 chr6: 82,277,979-83,297,975	TPBG, LOC105377876, 8 more genes
nsv6636874	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 81,087,736-84,200,632 , GRCh38.p12 chr6: 80,378,019-83,490,913	TPBG, PGM3, 24 more genes

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