endog[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
nsv3899776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 129,370,440-133,866,894 , GRCh38.p12 chr9: 126,608,161-130,991,507	ENDOG, FNBP1, 136 more genes
nsv3917587	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 127,795,683-131,484,475 , GRCh38 chr9: 125,993,583-129,682,375 , GRCh37 chr9: 128,755,862-132,444,654	ENDOG, DYNC2I2, 115 more genes
nsv3918361	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 129,676,681-132,287,019 , GRCh38 chr9: 127,874,581-130,421,811 , GRCh37 chr9: 130,636,860-133,297,198	ENDOG, GOLGA2, 89 more genes
nsv3903209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,390,139-132,760,275 , GRCh38.p12 chr9: 127,627,860-129,997,996	ENDOG, PTRH1, 99 more genes
nsv3909918	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 129,933,505-131,594,414 , GRCh37.p13 chr9: 130,893,684-132,554,593 , GRCh38.p12 chr9: 128,131,405-129,792,314	ENDOG, C9orf50, 65 more genes
nsv4675731	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,957,344-132,310,210 , GRCh38.p12 chr9: 128,195,065-129,547,931	ENDOG, PTPA, 55 more genes
nsv3914825	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 129,873,497-130,897,002 , GRCh37.p13 chr9: 130,833,676-131,857,181 , GRCh38.p12 chr9: 128,071,397-129,094,902	ENDOG, RNU7-171P, 49 more genes
nsv3924593	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 130,038,447-130,714,167 , GRCh38 chr9: 128,236,347-128,912,067 , GRCh37 chr9: 130,998,626-131,674,346	ENDOG, LRRC8A, 34 more genes
nsv3912247	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981	ENDOG, ALOX15P2, 2184 more genes
nsv3890420	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,122,247 , GRCh38.p12 chr9: 10,590-138,231,797	ENDOG, TBC1D13, 2183 more genes
nsv3905118	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,114,095 , GRCh38.p12 chr9: 10,590-138,223,645	ENDOG, MIR219A2, 2183 more genes
nsv3891842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,107,672 , GRCh38.p12 chr9: 10,590-138,217,222	ENDOG, OR13C1P, 2183 more genes
nsv3895453	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 46,587-141,066,491 , GRCh38.p12 chr9: 46,587-138,172,039	ENDOG, RPL19P15, 2176 more genes
nsv3900967	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 163,131-141,122,114 , GRCh38.p12 chr9: 163,131-138,231,664	ENDOG, BANCR, 2173 more genes
nsv3907479	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 62,525-141,006,407 , GRCh38.p12 chr9: 62,525-138,111,955	ENDOG, OR2AM1P, 2174 more genes
nsv3922684	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897	ENDOG, TDRD7, 2170 more genes
nsv3919257	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 204,193-141,073,897 , GRCh38 chr9: 204,193-138,179,445 , NCBI36 chr9: 194,193-140,193,718	ENDOG, LOC107987031, 2169 more genes
nsv3915973	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr9: 193,412-138,159,073 , GRCh37 chr9: 68,420,641-141,053,525 , NCBI36 chr9: 67,910,461-140,173,346	ENDOG, CTNNAL1, 2170 more genes
nsv3911025	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 193,412-138,124,524 , NCBI36 chr9: 194,090-140,138,797 , GRCh37 chr9: 204,090-141,018,976	ENDOG, RORB-AS1, 2168 more genes
nsv3921598	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389	ENDOG, PGAP4, 2167 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 44

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 44

Page of 3

Number of Variants: 20

Page of 3

Supplemental Content

Find related data

Search details

Recent activity