lowest common multiple - 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
nsv3878302	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 150,310,209-150,350,179 , GRCh37 chr4: 151,231,361-151,271,331	LRBA
nsv3887450	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 50,435,843-50,452,713 , GRCh38 chr7: 50,368,145-50,385,015	IKZF1
nsv4682321	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 151,814,184-151,818,990 , GRCh38.p12 chr4: 150,893,032-150,897,838	LRBA
nsv6634309	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 204,819,752-204,821,568 , GRCh38 chr2: 203,955,029-203,956,845	ICOS
nsv4681300	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 151,656,390-151,656,538 , GRCh38.p12 chr4: 150,735,238-150,735,386	LRBA
nsv6311907	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 151,814,184-151,814,321 , GRCh38.p12 chr4: 150,893,032-150,893,169	LRBA
nsv4682080	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 151,682,915-151,683,019 , GRCh38.p12 chr4: 150,761,763-150,761,867	LRBA
nsv5673648	copy number variation	2	nstd102	human	Pathogenic, Likely pathogenic	GRCh37 chr4: 151,604,683-151,604,889 , GRCh38.p12 chr4: 150,683,531-150,683,737	LRBA
nsv6309969	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr17: 16,875,309-16,875,389 , GRCh38.p12 chr17: 16,971,995-16,972,075	TNFRSF13B
nsv3917634	delins	1	nstd102	human	Pathogenic	GRCh37 chr16: 28,950,266-28,950,293 , GRCh38 chr16: 28,938,945-28,938,972	CD19
nsv5672868	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr17: 16,842,841-16,855,917 , GRCh38.p12 chr17: 16,939,527-16,952,603	TNFRSF13B
nsv7093256	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 151,849,088-151,849,741 , GRCh38 chr4: 150,927,936-150,928,589	LRBA
nsv6638071	delins	1	nstd102	human	Likely pathogenic	GRCh38 chr2: 203,870,707-203,870,773 , GRCh37 chr2: 204,735,430-204,735,496	CTLA4
nsv4453007	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 151,656,390-151,850,237 , GRCh38 chr4: 150,735,238-150,929,085	LRBA
nsv7096835	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 151,765,232-151,850,237 , GRCh38.p12 chr4: 150,844,080-150,929,085	LRBA
nsv6312239	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 151,719,213-151,753,148 , GRCh38.p12 chr4: 150,798,061-150,831,996	LRBA
nsv6311367	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 204,820,339-204,824,322 , GRCh38.p12 chr2: 203,955,616-203,959,599	ICOS
nsv7096982	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 151,849,648-151,850,237 , GRCh38.p12 chr4: 150,928,496-150,929,085	LRBA
nsv4453791	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr4: 150,921,178-150,921,313 , GRCh37 chr4: 151,842,330-151,842,465	LRBA
nsv6312238	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 151,186,874-151,247,070 , GRCh38.p12 chr4: 150,265,722-150,325,918	LRBA

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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 58

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Number of Variants: 20

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Supplemental Content

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