MMP16[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
nsv3894529	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 89,188,454-89,222,426 , GRCh38.p12 chr8: 88,176,225-88,210,197	MMP16
nsv3892619	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 89,098,320-89,103,325 , GRCh38.p12 chr8: 88,086,092-88,091,097	MMP16
nsv3896475	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 89,098,320-89,100,061 , GRCh38.p12 chr8: 88,086,092-88,087,833	MMP16
nsv4729350	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 89,055,371-89,170,064 , GRCh38.p12 chr8: 88,043,143-88,157,835	MMP16
nsv4455910	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 88,989,315-89,115,278 , GRCh38.p12 chr8: 87,977,087-88,103,050	MMP16
nsv6637796	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 89,215,136-89,342,944 , GRCh38.p12 chr8: 88,202,907-88,330,715	MMP16, LOC105375630
nsv3911034	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 79,584,698-96,379,096 , NCBI36 chr8: 79,747,253-96,448,272 , GRCh38 chr8: 78,672,463-95,366,868	MMP16, LOC105375933, 233 more genes
nsv3914059	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 78,677,666-92,851,513 , GRCh38 chr8: 77,765,431-91,839,285 , NCBI36 chr8: 78,840,221-92,920,689	MMP16, RN7SL107P, 176 more genes
nsv7137123	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 89,179,899-97,978,274 , GRCh38.p12 chr8: 88,167,670-96,966,046	MMP16, SLC26A7, 112 more genes
nsv3915173	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636	MMP16, RN7SL474P, 2109 more genes
nsv3901821	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028	MMP16, TBC1D31, 2109 more genes
nsv4349554	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385	MMP16, LOC101929488, 2105 more genes
nsv3916777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575	MMP16, RPL5P22, 2105 more genes
nsv3898123	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385	MMP16, SPAG1, 2105 more genes
nsv3908608	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 164,984-146,293,414 , GRCh38.p12 chr8: 214,984-145,068,028	MMP16, LINC01617, 2105 more genes
nsv3893757	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,991-146,280,828 , GRCh38.p12 chr8: 208,991-145,055,442	MMP16, LOC105375890, 2105 more genes
nsv3923310	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098	MMP16, LOC112268023, 2105 more genes
nsv3914307	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 191,605-146,280,167 , GRCh38 chr8: 241,605-145,054,781 , NCBI36 chr8: 181,605-146,250,971	MMP16, LOC107986897, 2104 more genes
nsv3919282	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824	MMP16, MIR4662B, 2104 more genes
nsv3919200	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639	MMP16, LOC112268023, 2103 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 41

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Number of Variants: 20

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Supplemental Content

Find related data

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