stim2[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3881897	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 26,956,005-26,970,376 , GRCh38.p12 chr4: 26,954,383-26,968,754	STIM2
nsv3884705	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 26,945,149-26,957,436 , GRCh38.p12 chr4: 26,943,527-26,955,814	STIM2
nsv3874539	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 26,950,265-26,957,489 , GRCh38.p12 chr4: 26,948,643-26,955,867	STIM2
nsv3879938	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 26,900,670-27,025,497 , GRCh38.p12 chr4: 26,899,048-27,023,875	STIM2
nsv3914868	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 26,513,294-26,902,461 , GRCh37.p13 chr4: 26,904,196-27,293,363 , GRCh38.p12 chr4: 26,902,574-27,291,741	STIM2, LINC02261
nsv3877950	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 4,165,334-33,324,781 , GRCh38.p12 chr4: 4,163,607-33,323,159	STIM2, LOC100418700, 353 more genes
nsv3885762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 71,552-29,006,745 , GRCh38.p12 chr4: 71,660-29,005,123	STIM2, CD38, 456 more genes
nsv3923296	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 72,555-28,066,309 , NCBI36 chr4: 62,447-27,677,029 , GRCh37 chr4: 72,447-28,067,931	STIM2, OR7E99P, 446 more genes
nsv7098818	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 11,399,082-38,137,335 , GRCh37.p13 chr4: 11,400,706-38,138,956	STIM2, LOC105374542, 232 more genes
nsv6313559	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 19,892,850-37,325,128 , GRCh38.p12 chr4: 19,891,227-37,323,506	STIM2, LOC102723846, 135 more genes
nsv3911497	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 16,925,022-32,113,076 , NCBI36 chr4: 16,535,743-31,758,596 , GRCh37 chr4: 16,926,645-32,114,698	STIM2, LINC02506, 128 more genes
nsv4347528	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 12,778,849-27,760,141 , GRCh38.p12 chr4: 12,777,225-27,758,519	STIM2, MTCO3P44, 148 more genes
nsv4674448	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 20,406,475-29,134,345 , GRCh38.p12 chr4: 20,404,852-29,132,723	STIM2, LOC100288962, 84 more genes
nsv3881579	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 23,458,442-29,252,060 , GRCh38.p12 chr4: 23,456,819-29,250,438	STIM2, HNRNPA1P65, 67 more genes
nsv3920498	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 23,472,721-27,296,266 , GRCh38 chr4: 23,862,000-27,685,546 , GRCh37 chr4: 23,863,623-27,687,168	STIM2, RNU7-126P, 48 more genes
nsv3873978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724	STIM2, LOC100422029, 2358 more genes
nsv3876533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611	STIM2, LOC100420289, 2347 more genes
nsv3884499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286	STIM2, MTND4LP29, 2341 more genes
nsv3880085	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318	STIM2, LOC112268460, 2345 more genes
nsv3883791	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495	STIM2, LOC105377343, 2341 more genes

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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 40

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Number of Variants: 20

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