TIMP3 - 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
nsv4457471	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr22: 33,067,984-33,370,145 , GRCh38.p12 chr22: 32,671,998-32,974,160	TIMP3, SYN3
nsv3904013	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr22: 33,209,740-33,403,536 , GRCh38.p12 chr22: 32,813,754-33,007,551	TIMP3, SYN3
nsv5381318	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr22: 33,197,988-33,198,128 , GRCh38.p12 chr22: 32,802,002-32,802,142	TIMP3, SYN3
nsv7021371	copy number variation	1	nstd229	human		GRCh38 chr22: 32,836,758-33,010,060 , GRCh37.p13 chr22: 33,232,745-33,406,045	TIMP3, SYN3
nsv7032602	copy number variation	1	nstd229	human		GRCh38 chr22: 32,831,378-32,833,903 , GRCh37.p13 chr22: 33,227,364-33,229,889	TIMP3, SYN3
nsv6537097	copy number variation	1	nstd223	human		GRCh38 chr22: 32,852,005-32,872,737 , GRCh37.p13 chr22: 33,247,992-33,268,724	TIMP3, SYN3
nsv6551126	copy number variation	1	nstd223	human		GRCh38 chr22: 32,831,376-32,833,900 , GRCh37.p13 chr22: 33,227,362-33,229,886	TIMP3, SYN3
nsv6554505	copy number variation	1	nstd223	human		GRCh38 chr22: 32,846,452-32,847,258 , GRCh37.p13 chr22: 33,242,439-33,243,245	TIMP3, SYN3
nsv6551800	copy number variation	1	nstd223	human		GRCh38 chr22: 32,851,677-32,852,200 , GRCh37.p13 chr22: 33,247,664-33,248,187	TIMP3, SYN3
nsv6146327	copy number variation	1	nstd206	human		GRCh38 chr22: 32,843,972-32,844,023 , GRCh37.p13 chr22: 33,239,959-33,240,010	TIMP3, SYN3
nsv5036924	copy number variation	1	nstd200	human		GRCh38 chr22: 32,852,005-32,872,737 , GRCh37.p13 chr22: 33,247,992-33,268,724	TIMP3, SYN3
nsv5040829	copy number variation	1	nstd200	human		GRCh38 chr22: 32,831,366-32,833,911 , GRCh37.p13 chr22: 33,227,352-33,229,897	TIMP3, SYN3
nsv5037161	copy number variation	1	nstd200	human		GRCh38 chr22: 32,841,132-32,842,227 , GRCh37.p13 chr22: 33,237,119-33,238,214	TIMP3, SYN3
nsv4883794	copy number variation	1	nstd200	human		GRCh37 chr22: 33,237,119-33,238,214 , GRCh38.p12 chr22: 32,841,132-32,842,227	TIMP3, SYN3
nsv5035330	copy number variation	1	nstd200	human		GRCh38 chr22: 32,845,981-32,846,112 , GRCh37.p13 chr22: 33,241,968-33,242,099	TIMP3, SYN3
nsv4871860	copy number variation	1	nstd200	human		GRCh37 chr22: 33,241,968-33,242,099 , GRCh38.p12 chr22: 32,845,981-32,846,112	TIMP3, SYN3
nsv4533209	copy number variation	1	nstd166	human		GRCh37.p13 chr22: 33,227,363-33,229,888 , GRCh38.p12 chr22: 32,831,377-32,833,902	TIMP3, SYN3
nsv4283847	copy number variation	1	nstd166	human		GRCh37.p13 chr22: 33,208,753-33,209,514 , GRCh38.p12 chr22: 32,812,767-32,813,528	TIMP3, SYN3
nsv4289471	copy number variation	1	nstd166	human		GRCh37.p13 chr22: 33,246,290-33,246,698 , GRCh38.p12 chr22: 32,850,303-32,850,711	TIMP3, SYN3
nsv4287947	copy number variation	1	nstd166	human		GRCh37.p13 chr22: 33,241,968-33,242,099 , GRCh38.p12 chr22: 32,845,981-32,846,112	TIMP3, SYN3

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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 231

Page of 12

Number of Variants: 20

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Supplemental Content

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