mmp20[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
nsv6636030	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr11: 102,601,121-102,601,432 , GRCh37 chr11: 102,471,852-102,472,163	MMP20
nsv6314513	complex chromosomal rearrangement	2	nstd102	human	Uncertain significance	GRCh37 chr17: 22,245,536-22,245,536 , GRCh37 chr17: 22,245,671-22,245,671 , GRCh38.p12 chr17: 22,746,209-22,746,209 , GRCh38.p12 chr17: 22,746,344-22,746,344 , GRCh38.p12 chr16: 3,057,688-3,057,688 , GRCh38.p12 chr16: 3,057,864-3,057,864 , GRCh37 chr16: 3,107,689-3,107,689 , GRCh37 chr16: 3,107,865-3,107,865	MMP25, MMP25-AS1
nsv3896340	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 3,106,994-3,132,197 , GRCh38.p12 chr16: 3,056,993-3,082,196	MMP25-AS1, IL32, 3 more genes
nsv3896696	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 3,106,994-3,117,877 , GRCh38.p12 chr16: 3,056,993-3,067,876	IL32, MMP25, 2 more genes
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	MMP20, FAUP4, 2031 more genes
nsv3904761	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 80,053,454-113,316,236 , GRCh38.p12 chr11: 80,342,410-113,445,514	MMP20, RPS6P16, 449 more genes
nsv3913977	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 77,943,882-106,650,146 , GRCh38 chr11: 78,232,836-106,779,420 , NCBI36 chr11: 77,621,530-106,155,356	MMP20, PLS1P1, 349 more genes
nsv3910101	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 87,796,211-113,996,548 , GRCh37.p13 chr11: 88,156,563-114,491,338 , GRCh38.p12 chr11: 88,423,395-114,620,616	MMP20, PHB1P16, 385 more genes
nsv6637396	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313	MMP20, LOC107984375, 295 more genes
nsv3894488	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 88,152,458-109,414,650 , GRCh38.p12 chr11: 88,419,290-109,543,924	MMP20, RNU6-16P, 270 more genes
nsv3910663	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 91,086,659-109,595,582 , NCBI36 chr11: 90,459,475-108,971,518 , GRCh37 chr11: 90,819,827-109,466,308	MMP20, LOC101060084, 230 more genes
nsv3922508	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 85,242,847-102,920,097 , GRCh37 chr11: 84,953,891-102,738,968 , NCBI36 chr11: 84,631,539-102,296,037	MMP20, AMOTL1, 240 more genes
nsv5672640	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976	MMP20, HSPD1P13, 239 more genes
nsv6637687	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 101,371,503-109,306,519 , GRCh38.p12 chr11: 101,500,772-109,435,793	MMP20, GRIA4, 111 more genes
nsv3924464	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 97,733,839-105,435,083 , GRCh38 chr11: 98,357,901-106,059,146 , GRCh37 chr11: 98,228,629-105,929,873	MMP20, ARHGAP42, 91 more genes
nsv3912877	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,900,735-7,160,698 , NCBI36 chr16: 2,840,736-7,100,699 , GRCh38 chr16: 2,850,734-7,110,697	TRP-CGG1-2, RBFOX1, 129 more genes
nsv6309019	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 101,323,686-103,349,981 , GRCh38.p12 chr11: 101,452,955-103,479,253	MMP20, RPL21P96, 40 more genes
nsv3911457	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,544,805-3,296,579 , GRCh38 chr16: 2,494,804-3,246,579 , NCBI36 chr16: 2,484,806-3,236,580	SNORA3C, PKMYT1, 70 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	MMP20, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	MMP20, RTN3, 2833 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 71

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Number of Variants: 20

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