dpy30[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
nsv1398625	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 32,035,374-32,122,619 , GRCh37 chr2: 32,260,443-32,347,688	DPY30, SPAST
nsv1398051	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 32,038,850-32,108,653 , GRCh37 chr2: 32,263,919-32,333,722	DPY30, SPAST
nsv4454242	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr2: 32,249,793-32,366,153 , GRCh38.p12 chr2: 32,024,724-32,141,084	DPY30, SPAST
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	DPY30, 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	DPY30, 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	DPY30, LOC105374435, 71 more genes
nsv3885614	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 29,240,004-32,380,876 , GRCh38.p12 chr2: 29,017,138-32,155,807	DPY30, LOC107985861, 32 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	DPY30, ATP6V0E1P3, 30 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	DPY30, LOC107985863, 14 more genes
nsv3890241	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 31,445,002-32,166,202 , GRCh37 chr2: 31,591,498-32,312,698 , GRCh38 chr2: 31,368,632-32,087,629	DPY30, SPAST, 8 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	DPY30, 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	DPY30, 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	DPY30, 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	DPY30, 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	DPY30, 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	DPY30, 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	DPY30, 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	DPY30, LOC105373394, 507 more genes
nsv3875055	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 27,861,707-60,790,985 , GRCh38.p12 chr2: 27,638,840-60,563,850	DPY30, RPL7P13, 426 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	DPY30, ATL2, 465 more genes

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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 32

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Number of Variants: 20

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