sox2[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
nsv4769297	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,902,731-182,945,128 , GRCh38.p12 chr3: 183,184,943-183,227,340	MCF2L2
nsv3880715	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 180,797,921-180,852,711 , GRCh38.p12 chr3: 181,080,133-181,134,923	SOX2-OT
nsv3885467	copy number variation	1	nstd102	human	Benign	GRCh37 chr3: 180,852,155-180,852,711 , GRCh38.p12 chr3: 181,134,367-181,134,923	SOX2-OT
nsv3924930	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 182,227,158-182,389,776 , GRCh37.p13 chr3: 180,744,464-180,907,082 , GRCh38.p12 chr3: 181,026,676-181,189,294	SOX2-OT
nsv4674364	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 181,386,449-181,504,204 , GRCh38.p12 chr3: 181,668,661-181,786,416	SOX2, SOX2-OT
nsv3917117	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 182,889,729-182,994,598 , GRCh38 chr3: 181,689,247-181,794,116 , GRCh37 chr3: 181,407,035-181,511,904	SOX2, SOX2-OT
nsv3912655	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 181,710,887-181,748,657 , NCBI36 chr3: 182,911,369-182,949,139 , GRCh37 chr3: 181,428,675-181,466,445	SOX2, SOX2-OT
nsv997224	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chr3: 181,429,712-181,432,224 , GRCh38.p12 chr3: 181,711,924-181,714,436	SOX2, SOX2-OT
nsv3915871	copy number variation	1	nstd102	human	Benign	NCBI36 chr3: 182,845,473-182,952,205 , GRCh37 chr3: 181,362,779-181,469,511 , GRCh38 chr3: 181,644,991-181,751,723	SOX2, SOX2-OT
nsv3917522	copy number variation	1	nstd102	human	Benign	NCBI36 chr3: 182,912,642-182,913,647 , GRCh37 chr3: 181,429,948-181,430,953 , GRCh38 chr3: 181,712,160-181,713,165	SOX2, SOX2-OT
nsv3883237	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 181,430,129-181,592,675 , GRCh38 chr3: 181,712,341-181,874,887	SOX2, RNA5SP150, 2 more genes
nsv4769326	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 182,871,341-182,987,855 , GRCh38.p12 chr3: 183,153,553-183,270,067	LAMP3, RNA5SP151, 3 more genes
nsv3912639	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 182,705,068-183,488,303 , GRCh37 chr3: 181,222,374-182,005,609 , GRCh38 chr3: 181,504,586-182,287,821	SOX2, SOX2-OT, 7 more genes
nsv4769323	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 180,913,778-181,432,287 , GRCh38.p12 chr3: 181,195,990-181,714,499	SOX2, SOX2-OT, 4 more genes
nsv3914166	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 180,856,452-192,229,812 , GRCh38 chr3: 181,138,664-192,512,023 , NCBI36 chr3: 182,339,146-193,712,506	SOX2, SNORA4, 199 more genes
nsv3913254	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 175,313,014-183,652,825 , GRCh37.p13 chr3: 173,830,320-182,170,131 , GRCh38.p12 chr3: 174,112,530-182,452,343	SOX2, RNU6-486P, 88 more genes
nsv6634384	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 181,062,175-185,474,509 , GRCh38.p12 chr3: 181,344,387-185,756,721	SOX2, PRICKLE1P1, 99 more genes
nsv4769252	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 181,171,210-184,706,091 , GRCh38.p12 chr3: 181,453,422-184,988,303	SOX2, LOC107986054, 83 more genes
nsv4769308	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 180,834,336-183,551,661 , GRCh38.p12 chr3: 181,116,548-183,833,873	SOX2, SNORD3P4, 43 more genes
nsv6634512	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 179,547,548-182,152,788 , GRCh37.p13 chr3: 179,265,336-181,870,576	SOX2, LOC105374243, 34 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 47

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Number of Variants: 20

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Supplemental Content

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