trim54[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
nsv6634330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419	TRIM54, CYP1B1-AS1, 1649 more genes
nsv3890734	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 22,656,029-28,601,557 , GRCh37 chr2: 22,802,524-28,748,053 , GRCh38 chr2: 22,579,652-28,525,186	TRIM54, MAPRE3-AS1, 142 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	TRIM54, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	TRIM54, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	TRIM54, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	TRIM54, MTND2P22, 3724 more genes
nsv3908605	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 66,097-55,797,773 , GRCh38 chr2: 66,097-55,570,637 , NCBI36 chr2: 56,097-55,651,277	TRIM54, SLC35F6, 801 more genes
nsv3908288	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 236,816-46,210,371 , GRCh38 chr2: 236,816-45,983,232 , NCBI36 chr2: 226,816-46,063,875	TRIM54, ALLC, 674 more genes
nsv6636815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573	TRIM54, LOC105374455, 504 more genes
nsv3908038	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 12,770-33,936,576 , NCBI36 chr2: 2,770-33,790,080 , GRCh38 chr2: 12,770-33,711,509	TRIM54, LOC105373394, 507 more genes
nsv3879320	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 22,665,048-52,850,368 , GRCh38.p12 chr2: 22,442,176-52,623,230	TRIM54, ATL2, 465 more genes
nsv3907033	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 20,341-28,496,035 , GRCh38 chr2: 30,341-28,419,664 , GRCh37 chr2: 30,341-28,642,531	TRIM54, GTF3C2-AS1, 434 more genes
nsv6137788	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145	TRIM54, GTF3C2-AS1, 316 more genes
nsv3919769	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 22,776,056-33,845,581 , GRCh37.p13 chr2: 22,922,551-33,992,077 , GRCh38.p12 chr2: 22,699,679-33,767,010	TRIM54, RNA5SP88, 213 more genes
nsv6112680	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 24,881,528-43,460,021 , GRCh38.p12 chr2: 24,658,659-43,232,882	TRIM54, ADCY3, 314 more genes
nsv3903805	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 7,635,254-88,005,418 , NCBI36 chr2: 7,552,705-87,786,533 , GRCh38 chr2: 7,495,123-87,705,899	TRIM54, LOC101927723, 1246 more genes
nsv4674559	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 27,519,013-27,610,482 , GRCh38.p12 chr2: 27,296,145-27,387,615	TRIM54, GTF3C2-AS2, 8 more genes
nsv7096625	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 24,443,763-30,143,525 , GRCh38.p12 chr2: 24,220,894-29,920,659	TRIM54, LOC105374381, 136 more genes
nsv7096148	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr2: 24,443,763-29,022,169 , GRCh38.p12 chr2: 24,220,894-28,799,303	TRIM54, LOC105374381, 122 more genes
nsv3896933	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr2: 25,835,975-27,374,008 , GRCh38 chr2: 25,759,602-27,297,636 , GRCh37 chr2: 25,982,471-27,520,504	TRIM54, CAD, 48 more genes

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Items: 20

Number of Variants: 20

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