srd5a3[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
nsv6311728	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 56,225,493-56,225,675 , GRCh38.p12 chr4: 55,359,326-55,359,508	SRD5A3
nsv3871446	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 56,225,485-56,300,646 , GRCh38.p12 chr4: 55,359,318-55,434,479	SRD5A3, TMEM165, 3 more genes
nsv5674237	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872	SRD5A3, FTLP10, 335 more genes
nsv3917232	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 54,759,525-62,818,428 , GRCh38 chr4: 54,198,601-62,270,115 , GRCh37 chr4: 55,064,768-63,135,833	SRD5A3, CLOCK, 84 more genes
nsv3912235	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 52,639,018-59,984,479 , GRCh37 chr4: 53,505,185-60,850,197 , NCBI36 chr4: 53,199,942-60,532,792	SRD5A3, LOC105377672, 97 more genes
nsv6291206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,685,685-58,104,722 , GRCh38.p12 chr4: 51,819,519-57,238,556	SRD5A3, DCUN1D4, 96 more genes
nsv6315421	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 53,688,710-56,491,447 , GRCh38.p12 chr4: 52,822,543-55,625,280	SRD5A3, METTL5P3, 38 more genes
nsv7097256	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr4: 55,124,936-57,368,027 , GRCh38.p12 chr4: 54,258,769-56,501,861	SRD5A3, AASDH, 40 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	SRD5A3, 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	SRD5A3, 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	SRD5A3, 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	SRD5A3, 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	SRD5A3, LOC105377343, 2341 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	SRD5A3, SNHG27, 1091 more genes
nsv3872797	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-66,440,622 , GRCh38.p12 chr4: 68,453-65,574,904	SRD5A3, GNPDA2, 813 more genes
nsv7148157	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396	SRD5A3, OR7E84P, 764 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	SRD5A3, LOC105377297, 582 more genes
nsv3914335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 44,358,218-63,111,600 , NCBI36 chr4: 44,052,975-62,794,195 , GRCh38 chr4: 44,356,201-62,245,882	SRD5A3, RPL22P13, 178 more genes
nsv3910089	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 52,392,545-67,539,802 , GRCh37 chr4: 52,697,788-67,857,207 , GRCh38 chr4: 51,831,622-66,991,489	SRD5A3, LINC02260, 154 more genes
nsv3919213	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,766,026-60,850,197 , NCBI36 chr4: 52,460,783-60,532,792 , GRCh38 chr4: 51,899,860-59,984,479	SRD5A3, LNX1-AS1, 106 more genes

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Number of Variants: 20

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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 22

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Number of Variants: 20

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Supplemental Content

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Search details

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