ifngr1[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
nsv4728929	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 137,517,088-137,606,046 , GRCh38.p12 chr6: 137,195,951-137,284,909	IFNGR1
nsv7097813	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 137,519,168-137,528,234 , GRCh38.p12 chr6: 137,198,031-137,207,097	IFNGR1
nsv3896395	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 137,433,986-137,600,146 , GRCh38.p12 chr6: 137,112,849-137,279,009	IFNGR1, IL22RA2
nsv4350212	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 135,239,633-146,997,510 , GRCh38.p12 chr6: 134,918,495-146,676,374	IFNGR1, LOC100131041, 146 more genes
nsv3904441	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 133,077,239-143,761,582 , GRCh38.p12 chr6: 132,756,100-143,440,445	IFNGR1, SNORD101, 147 more genes
nsv3916499	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 136,359,437-146,708,473 , GRCh37.p13 chr6: 136,317,744-146,666,780 , GRCh38.p12 chr6: 135,996,606-146,345,644	IFNGR1, SLC35D3, 127 more genes
nsv6314818	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 134,838,331-142,160,056 , GRCh37.p13 chr6: 135,159,469-142,481,193	IFNGR1, PBOV1, 100 more genes
nsv6112726	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 133,810,210-140,046,615 , GRCh38.p12 chr6: 133,489,072-139,725,478	IFNGR1, SIMALR, 99 more genes
nsv4675250	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 133,817,341-140,038,401 , GRCh38.p12 chr6: 133,496,203-139,717,264	IFNGR1, ALDH8A1, 99 more genes
nsv6312142	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 137,143,759-138,202,456 , GRCh38.p12 chr6: 136,822,621-137,881,319	IFNGR1, SLC35D3, 16 more genes
nsv4683010	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 136,482,728-137,540,520 , GRCh38.p12 chr6: 136,161,590-137,219,383	IFNGR1, PDE7B, 17 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	IFNGR1, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	IFNGR1, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	IFNGR1, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	IFNGR1, ITPR3, 2905 more genes
nsv3919111	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637	IFNGR1, RNU6-770P, 810 more genes
nsv3911993	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 133,900,102-166,209,023 , GRCh38 chr6: 133,537,271-165,875,545 , GRCh37 chr6: 133,858,409-166,289,033	IFNGR1, LOC105369171, 418 more genes
nsv3915150	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 124,322,082-156,156,864 , GRCh37.p13 chr6: 124,280,383-156,115,172 , GRCh38.p12 chr6: 123,959,238-155,794,038	IFNGR1, KATNA1, 422 more genes
nsv3913689	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 121,373,749-146,289,101 , GRCh37.p13 chr6: 121,332,050-146,247,408 , GRCh38.p12 chr6: 121,010,904-145,926,272	IFNGR1, TPD52L1, 316 more genes
nsv3911164	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 135,720,981-155,817,943 , GRCh37 chr6: 135,679,288-155,776,251 , GRCh38 chr6: 135,358,150-155,455,117	IFNGR1, HYMAI, 263 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 24

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 24

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity