srpx2[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
nsv3887576	copy number variation	1	nstd102	human	Benign	GRCh37 chrX: 99,881,576-99,918,666 , GRCh38.p12 chrX: 100,626,579-100,663,669	SRPX2, TSPAN6
nsv3874186	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 99,899,163-99,926,296 , GRCh38 chrX: 100,644,166-100,671,299	SRPX2, SYTL4
nsv3899791	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chrX: 100,650,751-100,680,705 , GRCh37 chrX: 99,905,748-99,935,702 , NCBI36 chrX: 99,792,404-99,822,358	SRPX2, SYTL4
nsv4682226	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 99,901,300-99,926,004 , GRCh38.p12 chrX: 100,646,303-100,671,007	SRPX2, SYTL4
nsv4682857	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 99,551,255-99,905,882 , GRCh38.p12 chrX: 100,296,257-100,650,885	SRPX2, TNMD, 3 more genes
nsv4454976	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 99,430,457-100,047,314 , GRCh38.p12 chrX: 100,175,459-100,792,325	SRPX2, TSPAN6, 4 more genes
nsv3915917	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chrX: 99,551,255-99,926,004 , GRCh38.p12 chrX: 100,296,257-100,671,007	SRPX2, TSPAN6, 4 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	SRPX2, 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	SRPX2, 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	SRPX2, 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	SRPX2, 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	SRPX2, 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	SRPX2, 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	SRPX2, 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	SRPX2, 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	SRPX2, 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	SRPX2, 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	SRPX2, 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	SRPX2, 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	SRPX2, 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 174

Page of 9

Number of Variants: 20

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Supplemental Content

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Search details

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