srpk3[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
nsv7099008	copy number variation	1	nstd102	human	Pathogenic	GRCh37.p13 chrX\|NW_003871103.3: 1,148,346-1,215,630 , GRCh38 chrX: 153,714,363-153,781,647 , GRCh37.p13 chrX: 152,979,818-153,047,102	SRPK3, ABCD1, 3 more genes
nsv4769307	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 153,011,909-153,063,825 , GRCh38.p12 chrX: 153,746,455-153,798,370	SRPK3, SSR4, 3 more genes
nsv7093132	copy number variation	1	nstd102	human	Pathogenic	GRCh37.p13 chrX\|NW_003871103.3: 1,212,265-1,229,207 , GRCh38 chrX: 153,778,282-153,795,224 , GRCh37.p13 chrX: 153,043,737-153,060,679	SRPK3, IDH3G, 2 more genes
nsv3882878	copy number variation	1	nstd102	human	Likely benign	GRCh37 chrX: 153,051,135-153,059,077 , GRCh38.p12 chrX: 153,785,680-153,793,622	SRPK3, IDH3G, 1 more genes
nsv3878150	copy number variation	1	nstd102	human	Likely benign	GRCh37 chrX: 152,969,516-153,044,721 , GRCh38.p12 chrX: 153,704,061-153,779,266	SRPK3, PLXNB3-AS1, 3 more genes
nsv3883217	copy number variation	1	nstd102	human	Benign	GRCh37 chrX: 153,035,798-153,049,739 , GRCh38.p12 chrX: 153,770,343-153,784,284	SRPK3, IDH3G, 1 more genes
nsv3873641	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 153,012,011-153,064,295 , GRCh38.p12 chrX: 153,746,557-153,798,840	SRPK3, SSR4, 3 more genes
nsv3904162	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 10,001-156,030,895 , GRCh37 chrX: 60,001-155,260,560 , NCBI36 chrX: 1-154,913,754	SRPK3, NANOGNBP3, 2154 more genes
nsv3913255	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chrX: 701-154,913,754 , GRCh37.p13 chrX: 60,701-155,260,560 , GRCh38.p12 chrX: 10,701-156,030,895	SRPK3, NHS-AS1, 2154 more genes
nsv3907094	copy number variation	4	nstd102	human	Pathogenic	GRCh38 chrX: 10,679-156,022,206 , GRCh37 chrX: 60,679-155,251,871 , NCBI36 chrX: 679-154,905,065	SRPK3, GPR119, 2153 more genes
nsv3878553	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chrX: 60,262-155,245,765 , GRCh38.p12 chrX: 10,262-156,016,100	SRPK3, H2AB2, 2152 more genes
nsv3898149	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 20,297-156,026,127 , NCBI36 chrX: 10,297-154,908,986 , GRCh37 chrX: 70,297-155,255,792	SRPK3, OR3B1P, 2154 more genes
nsv3877395	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 71,267-155,255,839 , GRCh38.p12 chrX: 21,267-156,026,174	SRPK3, ARMCX2, 2154 more genes
nsv3884935	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 71,267-155,255,792 , GRCh38.p12 chrX: 21,267-156,026,127	SRPK3, NDUFB11, 2154 more genes
nsv3903061	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chrX: 679-154,896,026 , GRCh38 chrX: 10,679-156,013,167 , GRCh37 chrX: 60,679-155,242,832	SRPK3, SLC38A5, 2152 more genes
nsv3885865	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 70,297-155,246,585 , GRCh38.p12 chrX: 20,297-156,016,920	SRPK3, MIR1277, 2152 more genes
nsv6112690	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301	SRPK3, LOC105373176, 2151 more genes
nsv3907545	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 64,245-155,228,958 , NCBI36 chrX: 4,245-154,882,152 , GRCh38 chrX: 14,245-155,999,293	SRPK3, TMEM30BP1, 2151 more genes
nsv3884029	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 71,267-155,224,766 , GRCh38.p12 chrX: 21,267-155,995,101	SRPK3, SSX4B, 2150 more genes
nsv3898185	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chrX: 76,102-155,226,096 , NCBI36 chrX: 16,102-154,879,290 , GRCh38 chrX: 26,102-155,996,431	SRPK3, ANKRD11P2, 2151 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 238

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Number of Variants: 20

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