tyro3[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4455526	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 41,837,513-41,869,276 , GRCh38.p12 chr15: 41,545,315-41,577,078	TYRO3, ELOCP2
nsv3916249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189	TYRO3, H3P40, 1616 more genes
nsv3919468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189	TYRO3, RNU6-18P, 1442 more genes
nsv3903255	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 41,689,327-52,446,981 , GRCh38.p12 chr15: 41,397,129-52,154,784	TYRO3, RN7SKP101, 234 more genes
nsv3900281	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337	TYRO3, MYZAP, 1750 more genes
nsv3913581	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189	TYRO3, MIR4513, 1754 more genes
nsv3904086	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959	TYRO3, TMEM202, 1747 more genes
nsv3905138	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413	TYRO3, FES, 1738 more genes
nsv3892955	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr15: 22,770,422-102,429,112 , GRCh38.p12 chr15: 23,319,714-101,888,909	TYRO3, FAM81A, 1614 more genes
nsv3876912	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 31,115,047-102,354,857 , GRCh38.p12 chr15: 30,822,844-101,814,654	TYRO3, RNU6-953P, 1385 more genes
nsv3899559	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 41,745,084-102,354,798 , GRCh38.p12 chr15: 41,452,886-101,814,595	TYRO3, CILP, 1176 more genes
nsv4436396	complex substitution	1	nstd102	human	Pathogenic	GRCh38.p12 chr15: 34,346,036-41,764,885 , GRCh37 chr15: 34,638,237-42,057,083	TYRO3, ACTC1, 150 more genes
nsv4729715	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr15: 41,869,275-42,484,890 , GRCh38.p12 chr15: 41,577,077-42,192,692	TYRO3, SPTBN5, 18 more genes
nsv3918770	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189	TYRO3, SNRPCP18, 1622 more genes
nsv3918644	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189	TYRO3, SNORD116-23, 1622 more genes
nsv3911945	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 20,203,424-100,338,915 , GRCh37.p13 chr15: 22,652,060-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189	TYRO3, HDDC3, 1622 more genes
nsv3915210	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 28,207,117-100,338,915 , GRCh37.p13 chr15: 30,419,825-102,521,392 , GRCh38.p12 chr15: 30,127,622-101,981,189	TYRO3, RPL21P113, 1428 more genes
nsv3922157	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189	TYRO3, GCHFR, 1382 more genes
nsv5380758	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289	TYRO3, LOC105370794, 1173 more genes

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