immt[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6636870	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 86,276,346-86,373,271 , GRCh38.p12 chr2: 86,049,223-86,146,148	IMMT, POLR1A, 2 more genes
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	IMMT, DAZAP2P1, 2991 more genes
nsv6634330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419	IMMT, CYP1B1-AS1, 1649 more genes
nsv3877742	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 74,365,484-89,129,064 , GRCh38.p12 chr2: 74,138,357-88,829,551	IMMT, RNU6-561P, 253 more genes
nsv3886532	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 74,527,522-89,125,488 , GRCh38.p12 chr2: 74,300,395-88,825,975	IMMT, RNU6-561P, 249 more genes
nsv4451607	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 77,907,114-87,330,965 , GRCh38.p12 chr2: 77,679,988-87,103,842	IMMT, REEP1, 134 more genes
nsv6112750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 81,209,244-86,688,030 , GRCh38.p12 chr2: 80,982,120-86,460,907	IMMT, VAMP8, 86 more genes
nsv6313890	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 82,486,900-87,322,042 , GRCh38.p12 chr2: 82,259,776-87,094,919	IMMT, LOC105374836, 93 more genes
nsv3899461	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 85,014,686-88,826,619 , GRCh37 chr2: 85,241,809-89,126,132 , NCBI36 chr2: 85,095,320-88,907,247	IMMT, CD8A, 115 more genes
nsv7096524	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 85,766,411-86,564,633 , GRCh38.p12 chr2: 85,539,288-86,337,510	IMMT, GPR160P1, 27 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	IMMT, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	IMMT, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	IMMT, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	IMMT, MTND2P22, 3724 more genes
nsv3916821	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 47,701,031-86,783,356 , GRCh37.p13 chr2: 47,847,527-86,929,845 , GRCh38.p12 chr2: 47,620,388-86,702,722	IMMT, NAGK, 595 more genes
nsv3897079	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 77,025,216-90,282,666 , NCBI36 chr2: 77,105,850-90,982,989 , GRCh37 chr2: 77,252,342-91,619,262	IMMT, IGKV2D-18, 280 more genes
nsv6314726	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196	IMMT, ACTG2, 1713 more genes
nsv3899242	copy number variation	2	nstd102	human	Uncertain significance, Likely benign	NCBI36 chr2: 86,142,641-86,362,837 , GRCh37 chr2: 86,289,130-86,509,326 , GRCh38 chr2: 86,062,007-86,282,203	IMMT, POLR1A, 5 more genes
nsv3878112	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr2: 86,285,942-86,506,132 , GRCh38.p12 chr2: 86,058,819-86,279,009	IMMT, POLR1A, 5 more genes
nsv3883832	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr2: 86,285,942-86,506,131 , GRCh38.p12 chr2: 86,058,819-86,279,008	IMMT, POLR1A, 5 more genes

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

Send to:

Search results

Items: 1 to 20 of 43

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

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 43

Page of 3

Number of Variants: 20

Page of 3

Supplemental Content

Find related data

Search details

Recent activity