toe1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 17

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3874944	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 45,794,968-45,805,936 , GRCh38 chr1: 45,329,296-45,340,264	TOE1, MUTYH
nsv4682365	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr1: 45,805,881-45,809,328 , GRCh38.p12 chr1: 45,340,209-45,343,656	TOE1, MUTYH, 1 more genes
nsv4682150	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 45,794,978-45,809,328 , GRCh38.p12 chr1: 45,329,306-45,343,656	TOE1, TESK2, 1 more genes
nsv7095620	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 45,800,053-45,809,328 , GRCh38.p12 chr1: 45,334,381-45,343,656	TOE1, MUTYH, 1 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	TOE1, MARK1, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	TOE1, SNAP47, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	TOE1, RNU1-153P, 4887 more genes
nsv6313688	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139	TOE1, LOC107984940, 407 more genes
nsv3888489	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr1: 45,303,358-52,157,856 , GRCh38.p12 chr1: 44,837,686-51,692,184	TOE1, CDKN2C, 141 more genes
nsv4674088	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 45,386,263-45,982,314 , GRCh38.p12 chr1: 44,920,591-45,516,642	TOE1, EIF2B3, 17 more genes
nsv4436181	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532	TOE1, LINC01776, 1853 more genes
nsv3878135	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 33,241,563-46,663,513 , GRCh38.p12 chr1: 32,775,962-46,197,841	TOE1, LINC02786, 365 more genes
nsv7095531	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 44,257,753-46,663,493 , GRCh38.p12 chr1: 43,792,082-46,197,821	TOE1, AKR1A1, 87 more genes
nsv6314936	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 44,346,001-46,332,161 , GRCh38.p12 chr1: 43,880,329-45,866,489	TOE1, ZSWIM5, 79 more genes
nsv3881136	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 45,715,667-46,501,705 , GRCh38.p12 chr1: 45,249,995-46,036,033	TOE1, AKR1A1, 22 more genes
nsv3894172	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr1: 45,200,617-45,823,521 , GRCh38 chr1: 44,962,358-45,585,262 , GRCh37 chr1: 45,428,030-46,050,934	TOE1, EIF2B3, 18 more genes
nsv4682227	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 45,288,077-45,805,936 , GRCh38.p12 chr1: 44,822,405-45,340,264	TOE1, MUTYH, 14 more genes

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