dbVar for Gene (Select 100507406) - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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	SIMALR, MTFR2, 99 more genes
nsv4685709	copy number variation	1	nstd102	human	not provided	GRCh37 chr6: 135,936,688-140,660,269 , GRCh38.p12 chr6: 135,615,550-140,339,132	MAP7, RN7SKP299, 74 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	ALDH8A1, IL22RA2, 99 more genes
nsv4492061	mobile element insertion	1	nstd166	human		GRCh37.p13 chr6: 138,055,374-138,055,374 , GRCh38.p12 chr6: 137,734,237-137,734,237	LINC02539
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	LOC100131041, ADGB-DT, 146 more genes
nsv4330897	inversion	1	nstd166	human		GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351	, ACAT2, 894 more genes
nsv3919212	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 136,454,132-138,137,046 , GRCh37.p13 chr6: 136,412,439-138,095,353 , GRCh38.p12 chr6: 136,091,301-137,774,216	MAP3K5-AS1, LOC102723633, 25 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	RNU6-770P, MAP3K5-AS2, 810 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	SLC35D3, SHPRH, 127 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	KATNA1, RNF217-AS1, 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	TPD52L1, MESTP1, 316 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	LOC105369171, SHPRH, 418 more genes
nsv3911251	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr6: 136,630,655-137,791,240 , NCBI36 chr6: 136,993,486-138,154,070 , GRCh37 chr6: 136,951,793-138,112,377	SLC35D3, IL22RA2, 18 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	HYMAI, SMIM28, 263 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	SNORD101, MTFR2, 147 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	ITPR3, HSD17B8, 2905 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	SOD1P1, HLA-DPB1, 2905 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	RNU6-411P, LOC107986611, 2910 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	LOC105378061, MIR4640, 2914 more genes
esv4011098	complex chromosomal rearrangement	4	estd236	human		GRCh37 chr6: 48,385,249-154,434,404 , GRCh38.p12 chr6: 48,417,513-154,113,269	, ACTBP8, 1274 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:

Links from Gene

Items: 1 to 20 of 102

Number of Variants: 20

Send to:

Supplemental Content

Find related data

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

Links from Gene

Items: 1 to 20 of 102

Page of 6

Number of Variants: 20

Page of 6

Supplemental Content

Find related data

Recent activity