dbVar for OMIM (Select 125647) - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7097847	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 7,582,865-7,586,121 , GRCh38.p12 chr6: 7,582,632-7,585,888	DSP
nsv7097846	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 7,576,220-7,581,055 , GRCh38.p12 chr6: 7,575,987-7,580,822	DSP
nsv7097454	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 7,542,149-7,880,576 , GRCh38.p12 chr6: 7,541,916-7,880,343	DSP-AS1, RPL29P1, 6 more genes
nsv7097453	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr6: 7,542,149-7,542,338 , GRCh38.p12 chr6: 7,541,916-7,542,105	DSP-AS1, DSP
nsv7097089	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 7,582,855-7,586,131 , GRCh38.p12 chr6: 7,582,622-7,585,898	DSP
nsv7097088	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 7,567,563-7,584,301 , GRCh38.p12 chr6: 7,567,330-7,584,068	DSP
nsv6314233	delins	1	nstd102	human	Uncertain significance	GRCh38 chr6: 7,584,805-7,584,806 , GRCh37 chr6: 7,585,038-7,585,039	DSP
nsv6314225	insertion	1	nstd102	human	Pathogenic	GRCh37 chr6: 7,579,987-7,579,987 , GRCh38 chr6: 7,579,754-7,579,754	DSP
nsv6312506	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 7,579,782-7,581,194 , GRCh38.p12 chr6: 7,579,549-7,580,961	DSP
nsv6312505	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 7,565,582-7,568,149 , GRCh38.p12 chr6: 7,565,349-7,567,916	DSP
nsv6312504	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 7,542,149-7,586,111 , GRCh38.p12 chr6: 7,541,916-7,585,878	DSP-AS1, DSP
nsv6312410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 7,583,161-7,587,903 , GRCh38.p12 chr6: 7,582,928-7,587,670	DSP
nsv6312065	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 7,552,967-7,579,627 , GRCh38.p12 chr6: 7,552,734-7,579,394	DSP
nsv5674021	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 7,565,582-7,569,583 , GRCh38.p12 chr6: 7,565,349-7,569,350	DSP
nsv4682590	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 7,570,660-7,586,121 , GRCh38.p12 chr6: 7,570,427-7,585,888	DSP
nsv4458171	delins	3	nstd102	human	Pathogenic, Likely pathogenic	GRCh37 chr6: 7,583,166-7,587,903 , GRCh38 chr6: 7,582,933-7,587,670	DSP
nsv4454898	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 7,542,129-7,586,131 , GRCh38 chr6: 7,541,896-7,585,898	DSP-AS1, DSP
nsv4453102	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 7,541,906-7,585,888 , GRCh37 chr6: 7,542,139-7,586,121	DSP, DSP-AS1
nsv3886689	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 7,570,650-7,586,131 , GRCh38 chr6: 7,570,417-7,585,898	DSP

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dbVar for OMIM (Select 125647) (20)
dbVar
txid43992[Organism] (23)
BioSample
Mus musculus snail family zinc finger 2 (Snai2), mRNA
Mus musculus snail family zinc finger 2 (Snai2), mRNA
gi|1378577869|ref|NM_011415.3|

Nucleotide
Homo sapiens cell division cycle 25B (CDC25B), RefSeqGene on chromosome 20
Homo sapiens cell division cycle 25B (CDC25B), RefSeqGene on chromosome 20
gi|568384835|ref|NG_029040.2|

Nucleotide
Candidiasis
Candidiasis
Infection with a fungus of the genus CANDIDA. It is usually a superficial infection of the moist areas of the body and is generally caused by CANDIDA ALBICANS. (Dorland, 27th ...<br/>Year introduced: 1981

MeSH

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