tyk2[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
nsv6310455	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 10,463,090-10,465,305 , GRCh38.p12 chr19: 10,352,414-10,354,629	TYK2
nsv4682570	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 10,461,490-10,461,858 , GRCh38.p12 chr19: 10,350,814-10,351,182	TYK2
nsv6310272	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 10,461,510-10,461,858 , GRCh38.p12 chr19: 10,350,834-10,351,182	TYK2
nsv4681434	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 10,488,870-10,489,102 , GRCh38.p12 chr19: 10,378,194-10,378,426	TYK2
nsv6310273	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 10,488,870-10,489,082 , GRCh38.p12 chr19: 10,378,194-10,378,406	TYK2
nsv3922964	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 10,319,474-13,777,860 , NCBI36 chr19: 10,291,150-13,749,674 , GRCh37 chr19: 10,430,150-13,888,674	TYK2, SWSAP1, 164 more genes
nsv3922999	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 10,240,071-12,946,266 , GRCh37.p13 chr19: 10,379,071-13,085,266 , GRCh38.p12 chr19: 10,268,395-12,974,452	TYK2, ZNF433, 155 more genes
nsv3912242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 9,846,119-11,338,677 , GRCh38 chr19: 9,735,443-11,228,001 , NCBI36 chr19: 9,707,119-11,199,677	TYK2, PPAN, 68 more genes
nsv3900924	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 10,286,133-11,040,457 , GRCh38.p12 chr19: 10,175,457-10,929,781	TYK2, MIR4322, 38 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	TYK2, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	TYK2, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	TYK2, LENG8, 2408 more genes
nsv3898900	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 9,678,768-14,853,426 , GRCh38.p12 chr19: 9,568,092-14,742,614	TYK2, FBXL12, 253 more genes
nsv3923415	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 10,286,934-14,020,806 , GRCh37 chr19: 10,425,934-14,159,806 , GRCh38 chr19: 10,315,258-14,048,994	TYK2, MAN2B1, 182 more genes
nsv3920643	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 10,267,082-11,000,364 , NCBI36 chr19: 10,128,082-10,861,364 , GRCh38 chr19: 10,156,406-10,889,688	TYK2, MIR4748, 36 more genes
nsv3922509	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr19: 10,302,331-10,892,228 , GRCh37 chr19: 10,441,331-11,031,228 , GRCh38 chr19: 10,330,655-10,920,552	TYK2, CDKN2D, 26 more genes
nsv3920616	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr19: 8,802,823-13,303,041 , GRCh37 chr19: 8,941,823-13,442,041 , GRCh38 chr19: 8,831,147-13,331,227	TYK2, ACP5, 236 more genes
nsv4457721	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 10,441,330-10,977,962 , GRCh38.p12 chr19: 10,330,654-10,867,286	TYK2, CDKN2D, 24 more genes
nsv6291543	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 9,941,033-11,739,567 , GRCh38.p12 chr19: 9,830,357-11,628,752	TYK2, KRI1, 88 more genes

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