tbc1d20[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3885368	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 435,480-448,074 , GRCh37.p13 chr20: 416,124-428,718	TBC1D20
nsv6311234	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 419,230-428,738 , GRCh38.p12 chr20: 438,586-448,094	TBC1D20
nsv7095897	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 401,495-443,049 , GRCh38.p12 chr20: 420,851-462,405	TBC1D20, RBCK1
nsv4768382	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 378,136-547,319 , GRCh38.p12 chr20: 397,492-566,675	TBC1D20, CSNK2A1, 2 more genes
nsv3897376	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 371,723-573,424 , GRCh38.p12 chr20: 391,079-592,780	TBC1D20, CSNK2A1, 2 more genes
nsv4676339	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 371,723-488,334 , GRCh38.p12 chr20: 391,079-507,690	TBC1D20, RBCK1, 2 more genes
nsv3892475	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 404,406-488,433 , GRCh38.p12 chr20: 423,762-507,789	TBC1D20, RBCK1, 1 more genes
nsv6637401	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 404,407-611,731 , GRCh38.p12 chr20: 423,763-631,087	TBC1D20, RBCK1, 2 more genes
nsv6315567	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 453,176-822,262 , GRCh37.p13 chr20: 433,820-802,905	TBC1D20, CSNK2A1, 5 more genes
nsv6311232	copy number variation	3	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr20: 389,402-746,418 , GRCh38.p12 chr20: 408,758-765,774	TBC1D20, CSNK2A1, 6 more genes
nsv4676270	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,568-2,269,777 , GRCh38.p12 chr20: 80,927-2,289,131	TBC1D20, LOC100289473, 60 more genes
nsv3917810	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 121,781-2,290,194 , GRCh37 chr20: 102,422-2,270,840 , NCBI36 chr20: 50,422-2,218,840	TBC1D20, RAD21L1, 59 more genes
nsv1398608	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 71,023-2,129,746 , GRCh38.p12 chr20: 90,382-2,149,100	TBC1D20, SIRPB3P, 58 more genes
nsv3899121	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 121,521-2,073,612 , GRCh38.p12 chr20: 140,880-2,092,966	TBC1D20, RN7SL561P, 56 more genes
nsv3914701	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 70,580-1,919,864 , NCBI36 chr20: 18,580-1,867,864 , GRCh38 chr20: 89,939-1,939,218	TBC1D20, MIR6869, 54 more genes
nsv3916212	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr20: 18,580-1,781,123 , GRCh37 chr20: 70,580-1,833,123 , GRCh38 chr20: 89,939-1,852,477	TBC1D20, NRSN2-AS1, 52 more genes
nsv3907056	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,568-1,823,540 , GRCh38.p12 chr20: 80,927-1,842,894	TBC1D20, ACTG1P3, 52 more genes
nsv3923563	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 18,580-1,699,213 , GRCh37 chr20: 70,580-1,751,213 , GRCh38 chr20: 89,939-1,770,567	TBC1D20, LOC101929937, 50 more genes
nsv3924759	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 18,580-1,422,759 , GRCh38 chr20: 89,939-1,494,113 , GRCh37 chr20: 70,580-1,474,759	TBC1D20, DEFB127, 39 more genes
nsv3915146	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 18,580-1,288,754 , GRCh38 chr20: 89,939-1,360,110 , GRCh37 chr20: 70,580-1,340,754	TBC1D20, TMEM74B, 34 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 74

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Number of Variants: 20

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