smarcad1[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
nsv3888826	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 95,060,602-95,099,194 , GRCh38.p12 chr4: 94,139,451-94,178,043	SMARCAD1-DT
nsv3872584	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 95,060,602-95,081,378 , GRCh38.p12 chr4: 94,139,451-94,160,227	SMARCAD1-DT
nsv5564262	complex substitution	1	nstd102	human	Pathogenic	GRCh37.p13 chr4: 95,096,941-95,175,379 , GRCh38 chr4: 94,175,790-94,254,228	SMARCAD1, HMGB3P15, 1 more genes
nsv3911198	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 94,289,958-95,121,723 , GRCh38 chr4: 93,368,807-94,200,572 , NCBI36 chr4: 94,508,981-95,340,746	ATOH1, HMGB3P15, 3 more genes
nsv3923759	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 58,862,002-102,129,682 , GRCh37.p13 chr4: 59,167,245-101,910,659 , GRCh38.p12 chr4: 58,301,079-100,989,502	SMARCAD1, EREG, 530 more genes
nsv3923733	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 80,427,023-100,855,441 , GRCh37 chr4: 81,348,177-101,776,598 , NCBI36 chr4: 81,567,201-101,995,621	SMARCAD1, PDLIM5, 215 more genes
nsv7148241	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930	SMARCAD1, LOC105377327, 214 more genes
nsv3888958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 81,314,915-96,636,651 , GRCh38.p12 chr4: 80,393,761-95,715,500	SMARCAD1, LOC391674, 156 more genes
nsv3912429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 81,800,931-95,730,598 , NCBI36 chr4: 82,019,955-95,949,621 , GRCh38 chr4: 80,879,777-94,809,447	SMARCAD1, RNU6-469P, 152 more genes
nsv3885328	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 92,201,567-103,043,808 , GRCh38.p12 chr4: 91,280,416-102,122,651	SMARCAD1, TRMT10A, 86 more genes
nsv3910689	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 92,610,413-101,521,991 , GRCh37 chr4: 93,531,564-102,443,148 , NCBI36 chr4: 93,750,587-102,662,171	SMARCAD1, GRID2, 77 more genes
nsv3888291	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 90,005,204-96,971,785 , GRCh38.p12 chr4: 89,084,053-96,050,634	SMARCAD1, HMGB3P15, 33 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	SMARCAD1, 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	SMARCAD1, 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	SMARCAD1, 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	SMARCAD1, 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	SMARCAD1, LOC105377343, 2341 more genes
nsv3875534	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 93,071,152-190,957,473 , GRCh38.p12 chr4: 92,150,001-190,036,318	SMARCAD1, KLKB1, 1118 more genes
nsv6291432	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354	SMARCAD1, SNHG27, 1091 more genes
nsv3913811	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 51,831,622-97,505,618 , GRCh37 chr4: 52,697,788-98,426,769 , NCBI36 chr4: 52,392,545-98,645,792	SMARCAD1, LOC105377297, 582 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 28

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 28

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity