dbVar for OMIM (Select 615636) - dbVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from OMIM

Items: 16

loading data ...

Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7098181	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 67,976,634-68,071,392 , GRCh38.p12 chr8: 67,064,399-67,159,157	RNA5SP268, CSPP1
nsv7097907	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 68,015,252-68,015,390 , GRCh38.p12 chr8: 67,103,017-67,103,155	CSPP1
nsv7097804	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 68,070,662-68,071,392 , GRCh38.p12 chr8: 67,158,427-67,159,157	CSPP1
nsv7097668	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 67,976,634-68,658,364 , GRCh38.p12 chr8: 67,064,399-67,746,129	MTND4LP27, MTATP6P12, 14 more genes
nsv6312734	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 68,105,679-68,105,857 , GRCh38.p12 chr8: 67,193,444-67,193,622	ARFGEF1, CSPP1
nsv6312733	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr8: 68,024,187-68,044,335 , GRCh38.p12 chr8: 67,111,952-67,132,100	CSPP1
nsv6312732	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr8: 68,018,120-68,071,392 , GRCh38.p12 chr8: 67,105,885-67,159,157	CSPP1
nsv6312731	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 67,998,222-67,998,365 , GRCh38.p12 chr8: 67,085,987-67,086,130	CSPP1
nsv6312651	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 68,044,166-68,044,335 , GRCh38.p12 chr8: 67,131,931-67,132,100	CSPP1
nsv6312650	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 68,024,187-68,107,828 , GRCh38.p12 chr8: 67,111,952-67,195,593	NPM1P44, ARFGEF1, 1 more genes
nsv5381559	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 68,024,197-68,107,828 , GRCh38.p12 chr8: 67,111,962-67,195,593	NPM1P44, ARFGEF1, 1 more genes
nsv5381480	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 67,786,376-68,165,857 , GRCh38.p12 chr8: 66,874,141-67,253,622	NPM1P44, LOC100288001, 10 more genes
nsv4683049	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 68,024,207-68,130,373 , GRCh38.p12 chr8: 67,111,972-67,218,138	ARFGEF1, CSPP1, 1 more genes
nsv4681392	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 67,922,950-67,976,731 , GRCh38.p12 chr8: 67,010,715-67,064,496	LOC105375885, COPS5, 2 more genes
nsv4681034	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 68,105,699-68,105,837 , GRCh38.p12 chr8: 67,193,464-67,193,602	ARFGEF1, CSPP1
nsv3879757	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr8: 67,111,952-67,195,613 , GRCh37 chr8: 68,024,187-68,107,848	ARFGEF1, CSPP1, 1 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Recent activity

Clear Turn Off Turn On

dbVar for OMIM (Select 615636) (17)
dbVar

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)