sox3[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
nsv3902801	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chrX: 139,157,396-139,604,699 , GRCh37 chrX: 139,329,730-139,777,033 , GRCh38 chrX: 140,247,565-140,694,868	SOX3, EEDP1, 3 more genes
nsv3906248	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chrX: 139,175,245-139,570,920 , GRCh37 chrX: 139,347,579-139,743,254 , GRCh38 chrX: 140,265,414-140,661,089	SOX3, EEDP1, 2 more genes
nsv3913217	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chrX: 139,111,084-139,445,238 , GRCh37.p13 chrX: 139,283,418-139,617,572 , GRCh38.p12 chrX: 140,201,262-140,535,407	SOX3, LOC105373343, 3 more genes
nsv3922057	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chrX: 139,237,765-139,570,835 , GRCh37.p13 chrX: 139,410,099-139,743,169 , GRCh38.p12 chrX: 140,327,934-140,661,004	SOX3, LOC105373344, 2 more genes
nsv4674569	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 139,504,563-139,804,670 , GRCh38.p12 chrX: 140,422,398-140,722,505	SOX3, LOC105373344, 3 more genes
nsv3897334	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chrX: 140,427,884-140,719,116 , GRCh37 chrX: 139,510,049-139,801,281 , NCBI36 chrX: 139,337,715-139,628,947	SOX3, LOC105373344, 3 more genes
nsv3894500	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chrX: 139,513,068-139,699,790 , NCBI36 chrX: 139,340,734-139,527,456 , GRCh38 chrX: 140,430,903-140,617,625	SOX3, RPS17P17, 1 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	SOX3, 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	SOX3, 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	SOX3, 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	SOX3, 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	SOX3, 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	SOX3, 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	SOX3, 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	SOX3, 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	SOX3, 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	SOX3, 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	SOX3, 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	SOX3, 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	SOX3, 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 188

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Number of Variants: 20

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Supplemental Content

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Search details

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