nudt17[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
nsv3912840	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643	NUDT17, CRB1, 1608 more genes
nsv3903429	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 144,126,513-147,699,831 , GRCh38 chr1: 143,515,074-149,563,337 , GRCh37 chr1: 145,415,156-149,433,207	NUDT17, PDZK1, 216 more genes
nsv3892632	copy number variation	4	nstd102	human	Pathogenic	GRCh37 chr1: 145,747,242-149,155,026 , GRCh38 chr1: 143,515,074-149,076,087 , NCBI36 chr1: 144,458,599-147,421,650	NUDT17, LOC728989, 205 more genes
nsv6634349	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 145,157,447-148,016,122 , GRCh38.p12 chr1: 144,536,526-149,492,442	NUDT17, TRN-GTT10-1, 170 more genes
nsv3884385	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 146,089,268-149,376,652 , GRCh38.p12 chr1: 144,536,526-148,549,211 , GRCh38.p12 chr7: 58,093,723-62,429,627	NUDT17, LOC105371215, 151 more genes
nsv6290404	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 146,043,714-148,514,899 , GRCh38.p12 chr1: 144,536,526-148,549,211	NUDT17, TRN-GTT9-2, 150 more genes
nsv3888699	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 146,105,170-148,513,854 , GRCh38.p12 chr1: 144,536,526-148,549,211	NUDT17, LINC01731, 150 more genes
nsv3881108	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 145,770,679-148,519,140 , GRCh38.p12 chr1: 144,536,526-148,549,211	NUDT17, NBPF10, 150 more genes
nsv3879037	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 145,770,625-148,514,899 , GRCh38.p12 chr1: 144,536,526-148,549,211	NUDT17, TRN-GTT2-8, 150 more genes
nsv3875576	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 145,784,611-148,519,963 , GRCh38.p12 chr1: 144,536,526-148,549,211	NUDT17, LOC107985593, 150 more genes
nsv3874179	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 145,786,360-148,514,899 , GRCh38.p12 chr1: 144,536,526-148,549,211	NUDT17, LOC101929805, 150 more genes
nsv3899666	copy number variation	13	nstd102	human	Pathogenic, Pathogenic/Likely pathogenic	GRCh37 chr1: 145,987,156-148,545,520 , NCBI36 chr1: 144,698,513-146,812,144 , GRCh38 chr1: 145,215,697-149,076,087	NUDT17, ANKRD34A, 136 more genes
nsv3887640	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 145,580,669-149,095,000 , GRCh37.p13 chr1\|NW_003871055.3: 2,396,082-5,910,413	NUDT17, LOC107985593, 121 more genes
nsv7098839	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 146,405,854-147,597,284 , GRCh38.p12 chr1: 145,598,009-149,077,123	NUDT17, CCT8P1, 120 more genes
nsv3898635	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 145,215,697-148,534,530 , GRCh37 chr1: 145,451,329-148,309,094 , NCBI36 chr1: 144,162,686-146,675,718	NUDT17, GJA8, 125 more genes
nsv3886236	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 146,470,887-148,020,200 , GRCh38.p12 chr1: 145,386,563-148,492,647	NUDT17, RNVU1-6, 116 more genes
nsv3871498	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 145,430,995-148,427,734 , GRCh37.p13 chr1\|NW_003871055.3: 2,246,408-5,243,147	NUDT17, TRE-TTC6-1, 109 more genes
nsv3900422	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 145,376,675-147,860,552 , NCBI36 chr1: 144,088,032-146,327,176 , GRCh38 chr1: 145,601,946-148,572,213	NUDT17, RNVU1-1, 109 more genes
nsv3916137	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr1: 144,764,810-146,338,877 , GRCh37.p13 chr1: 146,053,453-147,872,253 , GRCh38.p12 chr1: 145,430,980-148,400,100	NUDT17, RNVU1-8, 107 more genes
nsv5200304	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 146,500,972-147,851,297 , GRCh38.p12 chr1: 145,430,980-148,371,305	NUDT17, RN7SL261P, 103 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 180

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 180

Page of 9

Number of Variants: 20

Page of 9

Supplemental Content

Find related data

Search details

Recent activity