dbVar for OMIM (Select 605921) - dbVar - NCBI

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

Links from OMIM

Items: 13

loading data ...

Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7094168	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 4,045,083-4,045,237 , GRCh38.p12 chr11: 4,023,853-4,024,007	STIM1
nsv7093688	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 4,112,492-4,113,028 , GRCh38.p12 chr11: 4,091,262-4,091,798	STIM1
nsv6309364	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 3,877,491-3,877,649 , GRCh38.p12 chr11: 3,856,261-3,856,419	MIR4687, STIM1
nsv6309213	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 4,076,736-4,076,887 , GRCh38.p12 chr11: 4,055,506-4,055,657	STIM1
nsv6309212	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 3,832,490-4,113,028 , GRCh38.p12 chr11: 3,811,260-4,091,798	STIM1-AS1, RHOG, 7 more genes
nsv6309195	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 3,877,501-4,113,028 , GRCh38.p12 chr11: 3,856,271-4,091,798	PPIAP40, RPS29P20, 4 more genes
nsv6309110	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 3,988,762-4,113,028 , GRCh38.p12 chr11: 3,967,532-4,091,798	STIM1, HNRNPA1P76, 2 more genes
nsv5564129	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 4,112,492-4,113,048 , GRCh38.p12 chr11: 4,091,262-4,091,818	STIM1
nsv4683294	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 3,877,481-4,113,048 , GRCh38.p12 chr11: 3,856,251-4,091,818	HNRNPA1P76, RPS29P20, 4 more genes
nsv4683274	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 3,877,481-3,877,659 , GRCh38.p12 chr11: 3,856,251-3,856,429	STIM1, MIR4687
nsv4683169	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 3,988,762-4,113,048 , GRCh38.p12 chr11: 3,967,532-4,091,818	STIM1, HMGN1P21, 2 more genes
nsv4682930	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 4,080,501-4,080,636 , GRCh38.p12 chr11: 4,059,271-4,059,406	STIM1
nsv4453974	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 3,877,481-4,113,048 , GRCh38 chr11: 3,856,251-4,091,818	STIM1, HMGN1P21, 4 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Recent activity

Clear Turn Off Turn On

dbVar for OMIM (Select 605921) (14)
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)