dbVar for Gene (Select 7078) - 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
nsv5974550	insertion	1	nstd209	human		GRCh38 chr22: 32,814,324-32,814,324 , GRCh37.p13 chr22: 33,210,310-33,210,310	SYN3, TIMP3
nsv5668712	insertion	1	nstd207	human		GRCh38 chr22: 32,814,324-32,814,324 , GRCh37.p13 chr22: 33,210,310-33,210,310	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
nsv5360511	translocation	1	nstd200	human		GRCh38 chr22: 32,843,976-32,843,976 , GRCh38 chr22: 32,843,858-32,843,858 , GRCh37.p13 chr22: 33,239,845-33,239,845 , GRCh37.p13 chr22: 33,239,963-33,239,963	SYN3, TIMP3
nsv5332881	translocation	1	nstd200	human		GRCh37 chr22: 33,239,845-33,239,845 , GRCh37 chr22: 33,239,963-33,239,963 , GRCh38.p12 chr22: 32,843,858-32,843,858 , GRCh38.p12 chr22: 32,843,976-32,843,976	SYN3, TIMP3
nsv5296199	copy number variation	1	nstd204	human		GRCh38.p13 chr22: 32,807,001-32,807,800 , GRCh37.p13 chr22: 33,202,987-33,203,786	TIMP3, SYN3
nsv5188198	mobile element insertion	1	nstd203	human		GRCh38 chr22: 32,801,094-32,801,110 , GRCh37.p13 chr22: 33,197,080-33,197,096	SYN3, TIMP3
nsv5040829	copy number variation	1	nstd200	human		GRCh38 chr22: 32,831,366-32,833,911 , GRCh37.p13 chr22: 33,227,352-33,229,897	SYN3, TIMP3
nsv5037161	copy number variation	1	nstd200	human		GRCh38 chr22: 32,841,132-32,842,227 , GRCh37.p13 chr22: 33,237,119-33,238,214	SYN3, TIMP3
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
nsv5035330	copy number variation	1	nstd200	human		GRCh38 chr22: 32,845,981-32,846,112 , GRCh37.p13 chr22: 33,241,968-33,242,099	SYN3, TIMP3
nsv4888629	copy number variation	1	nstd200	human		GRCh37 chr22: 33,222,980-33,223,662 , GRCh38.p12 chr22: 32,826,994-32,827,676	SYN3, TIMP3
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
nsv4871860	copy number variation	1	nstd200	human		GRCh37 chr22: 33,241,968-33,242,099 , GRCh38.p12 chr22: 32,845,981-32,846,112	SYN3, TIMP3
nsv4759438	insertion	1	nstd199	human		GRCh37 chr22: 33,210,305-33,210,305 , GRCh38.p12 chr22: 32,814,319-32,814,319	TIMP3, SYN3
nsv4729926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824	FBXO7, GTSE1, 1084 more genes
nsv4676292	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 30,654,764-51,197,838 , GRCh38.p12 chr22: 30,258,775-50,759,410	PDXP-DT, PDGFB, 550 more genes
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	SYN3, TIMP3
nsv4509236	mobile element insertion	1	nstd166	human		GRCh37.p13 chr22: 33,242,309-33,242,309 , GRCh38.p12 chr22: 32,846,322-32,846,322	SYN3, TIMP3
nsv4457771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410	IGLV3-27, XKR3, 1082 more genes

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Number of Variants: 20

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Items: 1 to 20 of 211

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Number of Variants: 20

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