b3gnt5[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
nsv4769326	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,871,341-182,987,855 , GRCh38.p12 chr3: 183,153,553-183,270,067	B3GNT5, LAMP3, 3 more genes
nsv3881736	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 182,970,805-183,082,549 , GRCh38.p12 chr3: 183,253,017-183,364,761	B3GNT5, LOC107986160, 2 more genes
nsv3914166	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 180,856,452-192,229,812 , GRCh38 chr3: 181,138,664-192,512,023 , NCBI36 chr3: 182,339,146-193,712,506	B3GNT5, SNORA4, 199 more genes
nsv3882335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,650,681-191,275,809 , GRCh38.p12 chr3: 182,932,893-191,558,020	B3GNT5, VPS8, 171 more genes
nsv6313539	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,189,525-187,212,935 , GRCh38.p12 chr3: 182,471,737-187,495,147	B3GNT5, ALG3, 133 more genes
nsv6634384	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 181,062,175-185,474,509 , GRCh38.p12 chr3: 181,344,387-185,756,721	B3GNT5, PRICKLE1P1, 99 more genes
nsv4728604	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,877,291-186,830,759 , GRCh38.p12 chr3: 183,159,503-187,112,971	B3GNT5, LOC105374253, 111 more genes
nsv4769252	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 181,171,210-184,706,091 , GRCh38.p12 chr3: 181,453,422-184,988,303	B3GNT5, LOC107986054, 83 more genes
nsv4769308	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 180,834,336-183,551,661 , GRCh38.p12 chr3: 181,116,548-183,833,873	B3GNT5, SNORD3P4, 43 more genes
nsv7096553	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr3: 182,733,226-184,094,097 , GRCh38.p12 chr3: 183,015,438-184,376,309	B3GNT5, DVL3, 51 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	B3GNT5, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	B3GNT5, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	B3GNT5, RPL23AP49, 2875 more genes
nsv3918981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446	B3GNT5, LINC02614, 1469 more genes
nsv3918692	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833	B3GNT5, LOC105374179, 785 more genes
nsv3874894	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 142,995,020-192,997,215 , GRCh38.p12 chr3: 143,276,178-193,279,426	B3GNT5, RNU6-901P, 673 more genes
nsv3918066	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 152,100,512-198,118,383 , NCBI36 chr3: 153,300,991-199,329,651 , GRCh37 chr3: 151,818,301-197,845,254	B3GNT5, LOC105374260, 696 more genes
nsv3918149	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 155,836,230-197,851,986 , GRCh38 chr3: 156,118,441-198,125,115 , NCBI36 chr3: 157,318,924-199,336,383	B3GNT5, LINC02031, 647 more genes
nsv3913128	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 156,321,878-198,113,452 , NCBI36 chr3: 157,522,361-199,324,720 , GRCh37 chr3: 156,039,667-197,840,323	B3GNT5, SNORA4, 644 more genes
nsv3914686	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 158,493,861-199,345,995 , GRCh37 chr3: 157,011,167-197,861,598 , GRCh38 chr3: 157,293,378-198,134,727	B3GNT5, RPL34P10, 625 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 37

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 37

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity