yipf4[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
nsv3876456	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 32,495,395-32,541,438 , GRCh38.p12 chr2: 32,270,326-32,316,369	YIPF4
nsv3883852	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 32,515,609-32,691,438 , GRCh38.p12 chr2: 32,290,540-32,466,370	YIPF4, BIRC6
nsv3972167	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr2: 32,514,528-32,806,011 , GRCh38.p12 chr2: 32,289,459-32,580,944	YIPF4, BIRC6, 2 more genes
nsv1398123	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 32,362,824-32,817,794 , GRCh38.p12 chr2: 32,137,755-32,592,727	YIPF4, SPAST, 7 more genes
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	YIPF4, CYP1B1-AS1, 1649 more genes
nsv6313619	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 29,899,368-42,441,440 , GRCh38.p12 chr2: 29,676,502-42,214,300	YIPF4, LOC107985870, 161 more genes
nsv4454991	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 29,940,473-36,813,297 , GRCh38.p12 chr2: 29,717,607-36,586,154	YIPF4, LOC105374435, 71 more genes
nsv4453170	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 31,958,977-33,946,495 , GRCh38.p12 chr2: 31,733,908-33,721,428	YIPF4, ATP6V0E1P3, 30 more genes
nsv1398102	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 32,348,594-33,632,523 , GRCh38.p12 chr2: 32,123,525-33,407,456	YIPF4, TYW1P1, 16 more genes
nsv3900856	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 31,446,551-32,591,340 , GRCh37 chr2: 31,593,047-32,737,836 , GRCh38 chr2: 31,370,181-32,512,769	YIPF4, LOC107985863, 14 more genes
nsv1397917	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 32,327,163-32,886,455 , GRCh38.p12 chr2: 32,102,094-32,661,388	YIPF4, MIR558, 9 more genes
nsv4347299	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 32,339,736-32,875,274 , GRCh38.p12 chr2: 32,114,667-32,650,207	YIPF4, TTC27, 9 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	YIPF4, 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	YIPF4, 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	YIPF4, 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	YIPF4, 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	YIPF4, 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	YIPF4, 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	YIPF4, 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	YIPF4, LOC105373394, 507 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 35

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Number of Variants: 20

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Supplemental Content

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