zbbx[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
nsv4673935	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 166,902,027-167,019,204 , GRCh38.p12 chr3: 167,184,239-167,301,416	ZBBX
nsv4728207	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 166,831,213-167,390,123 , GRCh38.p12 chr3: 167,113,425-167,672,335	ZBBX, WDR49, 3 more genes
nsv3916480	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 166,999,191-167,272,477 , NCBI36 chr3: 168,481,885-168,755,171 , GRCh38 chr3: 167,281,403-167,554,689	ZBBX, LOC105374197, 3 more genes
nsv4452794	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 165,603,872-168,796,960 , GRCh38.p12 chr3: 165,886,084-169,079,172	ZBBX, MTND4P17, 31 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	ZBBX, 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	ZBBX, 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	ZBBX, 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	ZBBX, LINC02614, 1469 more genes
nsv6637156	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502	ZBBX, H1-10, 846 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	ZBBX, 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	ZBBX, 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	ZBBX, 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	ZBBX, 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	ZBBX, 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	ZBBX, RPL34P10, 625 more genes
nsv3871065	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 158,980,631-197,766,890 , GRCh38.p12 chr3: 159,262,842-198,040,019	ZBBX, LINC02048, 599 more genes
nsv3912173	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 167,337,691-199,336,383 , GRCh37 chr3: 165,854,997-197,851,986 , GRCh38 chr3: 166,137,209-198,125,115	ZBBX, LOC105374277, 540 more genes
nsv3918784	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 147,160,353-178,240,319 , GRCh38 chr3: 147,442,566-178,522,531 , NCBI36 chr3: 148,643,043-179,723,013	ZBBX, LOC105374167, 394 more genes
nsv3889215	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 157,128,738-181,637,333 , GRCh38.p12 chr3: 157,410,949-181,919,545	ZBBX, NAALADL2, 274 more genes
nsv3913042	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 166,359,093-181,330,650 , GRCh37 chr3: 164,876,399-179,847,956 , GRCh38 chr3: 165,158,611-180,130,168	ZBBX, LOC105374211, 169 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 25

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 25

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity