cep162[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
nsv6637090	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 84,720,708-84,922,710 , GRCh38.p12 chr6: 84,010,989-84,212,992	CEP162, LINC02857, 1 more genes
nsv3921478	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 76,692,636-93,477,232 , GRCh38 chr6: 75,926,199-92,710,793 , GRCh37 chr6: 76,635,916-93,420,511	CEP162, SPACA1, 187 more genes
nsv3923528	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 84,604,741-99,376,910 , GRCh38 chr6: 83,838,303-98,822,313 , GRCh37 chr6: 84,548,022-99,270,189	CEP162, RNU4-72P, 157 more genes
nsv3914309	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 82,569,098-93,753,476 , NCBI36 chr6: 83,335,534-94,519,915 , GRCh37 chr6: 83,278,815-94,463,194	CEP162, ME1, 136 more genes
nsv3873582	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 83,319,012-91,907,669 , GRCh38.p12 chr6: 82,609,295-91,197,951	CEP162, LOC105377882, 117 more genes
nsv6290989	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 83,141,523-88,023,466 , GRCh38.p12 chr6: 82,431,806-87,313,748	CEP162, KRT18P30, 58 more genes
nsv7098884	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 82,828,591-86,578,811 , GRCh38.p12 chr6: 82,118,874-85,869,093	CEP162, LOC105377879, 47 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	CEP162, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	CEP162, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	CEP162, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	CEP162, ITPR3, 2905 more genes
nsv3919111	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637	CEP162, RNU6-770P, 810 more genes
nsv6313857	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492	CEP162, LOC101928570, 288 more genes
nsv3872975	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 81,261,418-97,796,269 , GRCh38.p12 chr6: 80,551,701-97,348,393	CEP162, ME1, 178 more genes
nsv3878881	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 84,348,873-85,052,572 , GRCh38.p12 chr6: 83,639,154-84,342,854	CEP162, SNAP91, 5 more genes
nsv3882752	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 84,348,995-85,043,919 , GRCh38.p12 chr6: 83,639,276-84,334,201	CEP162, SNAP91, 5 more genes
nsv3873754	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 84,356,242-85,043,919 , GRCh38.p12 chr6: 83,646,523-84,334,201	CEP162, SNAP91, 5 more genes
nsv6313778	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 84,632,996-85,244,556 , GRCh38.p12 chr6: 83,923,277-84,534,838	CEP162, CYB5R4, 7 more genes
nsv6634392	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297	CEP162, MTHFD2P2, 212 more genes
nsv7097097	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 84,765,038-86,267,798 , GRCh38.p12 chr6: 84,055,319-85,558,080	CEP162, MRAP2, 18 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 32

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 32

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity