alg9[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
nsv6309402	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 124,191,253-124,207,015 , GRCh38.p12 chr12: 123,706,706-123,722,468	ATP6V0A2, TCTN2, 2 more genes
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	ALG9, FAUP4, 2031 more genes
nsv3904761	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 80,053,454-113,316,236 , GRCh38.p12 chr11: 80,342,410-113,445,514	ALG9, RPS6P16, 449 more genes
nsv3910101	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 87,796,211-113,996,548 , GRCh37.p13 chr11: 88,156,563-114,491,338 , GRCh38.p12 chr11: 88,423,395-114,620,616	ALG9, PHB1P16, 385 more genes
nsv5672640	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976	ALG9, HSPD1P13, 239 more genes
nsv4455554	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 104,101,411-116,680,918 , GRCh38.p12 chr11: 104,230,683-116,810,202	ALG9, LINC02732, 198 more genes
nsv4675680	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 103,320,065-114,349,787 , GRCh38.p12 chr11: 103,449,337-114,479,065	ALG9, DRD2, 181 more genes
nsv4675323	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 105,699,599-114,524,876 , GRCh38.p12 chr11: 105,828,873-114,654,154	ALG9, RPSAP50, 155 more genes
nsv6637811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 109,328,787-116,414,966 , GRCh38.p12 chr11: 109,458,061-116,544,249	ALG9, LOC102723966, 129 more genes
nsv4683939	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr11: 111,171,709-111,965,694 , GRCh38.p12 chr11: 111,300,984-112,094,970	ALG9, FDXACB1, 34 more genes
nsv7093830	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 111,171,709-111,959,745 , GRCh38.p12 chr11: 111,300,984-112,089,021	ALG9, LOC100132078, 34 more genes
nsv7093915	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 111,171,709-111,958,707 , GRCh38.p12 chr11: 111,300,984-112,087,983	ALG9, CRYAB, 34 more genes
nsv7093916	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 111,657,121-111,922,093 , GRCh38.p12 chr11: 111,786,397-112,051,369	ALG9, RPL37AP8, 13 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	ALG9, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	ALG9, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	ALG9, IGHMBP2, 2829 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	ALG9, PYGM, 2125 more genes
nsv3898361	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202	ALG9, SESN3, 694 more genes
nsv3922253	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 100,219,331-134,910,140 , NCBI36 chr11: 99,724,541-134,415,350 , GRCh38 chr11: 100,348,599-135,040,246	ALG9, RPS27P19, 655 more genes
nsv6289927	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522	ALG9, IGSF9B, 592 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 26

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 26

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity