ca6[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
nsv3887997	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 8,986,476-9,043,357 , GRCh38.p12 chr1: 8,926,417-8,983,298	CA6, LOC112268261, 1 more genes
nsv6290672	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,466-17,525,065 , GRCh38.p12 chr1: 914,086-17,198,570	CA6, RPL9P11, 466 more genes
nsv7098827	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749	CA6, LOC107985467, 386 more genes
nsv3900501	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 3,006,193-17,688,934 , GRCh37 chr1: 2,922,757-18,015,429 , NCBI36 chr1: 2,912,617-17,888,016	CA6, MFFP1, 364 more genes
nsv3873030	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 746,608-15,077,159 , GRCh38.p12 chr1: 811,228-14,750,663	CA6, RN7SL451P, 376 more genes
nsv3900236	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 5,363,826-18,360,302 , GRCh37 chr1: 5,423,886-18,686,796 , NCBI36 chr1: 5,323,746-18,559,383	CA6, PDPN, 333 more genes
nsv3888433	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-12,699,337 , GRCh38.p12 chr1: 82,154-12,639,316	CA6, AURKAIP1, 356 more genes
nsv6636785	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 6,758,933-19,287,770 , GRCh38.p12 chr1: 6,698,873-18,961,276	CA6, GPR157, 313 more genes
nsv4436105	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-11,784,118 , GRCh38.p12 chr1: 82,154-11,724,061	CA6, PARK7, 325 more genes
nsv3899046	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 844,347-12,470,133 , GRCh37 chr1: 779,727-12,530,188 , NCBI36 chr1: 769,590-12,452,775	CA6, PRKCZ-DT, 315 more genes
nsv6637093	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897	CA6, VWA1, 311 more genes
nsv3905483	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 6,303,641-15,799,093 , NCBI36 chr1: 6,286,288-15,998,175 , GRCh37 chr1: 6,363,701-16,125,588	CA6, VPS13D, 240 more genes
nsv6315409	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,466-10,258,804 , GRCh38.p12 chr1: 914,086-10,198,746	CA6, VAMP3, 245 more genes
nsv4436631	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 554,375-9,779,842 , GRCh38.p12 chr1: 618,995-9,719,784	CA6, LINC02606, 253 more genes
nsv3907841	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 837,491-9,616,363 , GRCh38 chr1: 902,111-9,556,305 , NCBI36 chr1: 827,354-9,538,950	CA6, PRKCZ-AS1, 224 more genes
nsv3890178	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 839,329-9,549,767 , GRCh37 chr1: 849,466-9,627,180 , GRCh38 chr1: 914,086-9,567,122	CA6, ANKRD65, 224 more genes
nsv3885408	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 4,558,588-13,187,457 , GRCh38.p12 chr1: 4,498,528-13,119,984	CA6, PRAMEF2, 198 more genes
nsv3909850	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 846,680-9,389,984 , GRCh38 chr1: 911,300-9,329,925 , NCBI36 chr1: 836,543-9,312,571	CA6, LOC105378590, 221 more genes
nsv3903444	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 4,958,499-13,178,528 , NCBI36 chr1: 4,858,359-13,101,115 , GRCh38 chr1: 4,898,439-13,111,056	CA6, NPPA-AS1, 195 more genes
nsv3896270	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 4,898,439-12,911,913 , NCBI36 chr1: 4,858,359-12,894,344 , GRCh37 chr1: 4,958,499-12,971,757	CA6, LINC01647, 185 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