sox18[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
nsv3902892	copy number variation	1	nstd102	human	Benign	GRCh37 chr20: 62,678,476-62,683,983 , GRCh38.p12 chr20: 64,047,123-64,052,630	SOX18, TCEA2
nsv3908513	copy number variation	1	nstd102	human	Benign	GRCh37 chr20: 62,679,468-62,681,617 , GRCh38.p12 chr20: 64,048,115-64,050,264	SOX18, TCEA2
nsv6314131	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,003,263-62,915,555 , GRCh38.p12 chr20: 62,428,207-64,284,202	SOX18, HAR1A, 100 more genes
nsv4676208	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,152,321-62,915,555 , GRCh38.p12 chr20: 62,555,114-64,284,202	SOX18, GMEB2, 94 more genes
nsv3916163	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,211,869-62,908,674 , GRCh38 chr20: 62,561,794-64,277,321 , NCBI36 chr20: 60,569,446-62,379,118	SOX18, LOC105372727, 94 more genes
nsv3916631	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,179,280-62,915,555 , NCBI36 chr20: 60,589,725-62,385,999 , GRCh38 chr20: 62,582,073-64,284,202	SOX18, PTK6, 91 more genes
nsv3922590	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 60,553,022-62,343,283 , GRCh38 chr20: 62,545,370-64,241,486 , GRCh37 chr20: 61,142,577-62,872,839	SOX18, RPL7P3, 95 more genes
nsv3913089	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 60,765,104-62,385,999 , GRCh37 chr20: 61,294,659-62,915,555 , GRCh38 chr20: 62,663,307-64,284,202	SOX18, SLCO4A1-AS1, 89 more genes
nsv3922908	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 61,010,752-62,435,964 , GRCh37.p13 chr20: 61,540,307-62,965,520 , GRCh38.p12 chr20: 62,908,955-64,334,167	SOX18, NPBWR2, 78 more genes
nsv6314091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,619,222-62,915,555 , GRCh38.p12 chr20: 62,987,870-64,284,202	SOX18, TPD52L2, 72 more genes
nsv6291738	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,775,756-62,915,555 , GRCh38.p12 chr20: 63,144,404-64,284,202	SOX18, PTK6, 63 more genes
nsv3911666	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,785,315-62,908,674 , GRCh38 chr20: 63,153,963-64,277,321 , NCBI36 chr20: 61,255,760-62,379,118	SOX18, MIR3196, 63 more genes
nsv3900085	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,827,144-62,907,526 , GRCh38.p12 chr20: 63,195,792-64,276,173	SOX18, PCMTD2, 62 more genes
nsv3909648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,827,144-62,907,467 , GRCh38.p12 chr20: 63,195,792-64,276,114	SOX18, LOC100130587, 62 more genes
nsv3909335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,884,113-62,915,555 , GRCh38.p12 chr20: 63,252,761-64,284,202	SOX18, TCEA2, 59 more genes
nsv4729740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,975,605-62,915,555 , GRCh38.p12 chr20: 63,344,253-64,284,202	SOX18, STMN3, 53 more genes
nsv3902622	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 62,002,369-62,915,555 , GRCh38.p12 chr20: 63,371,017-64,284,202	SOX18, ZGPAT, 53 more genes
nsv3895062	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 62,090,403-62,915,555 , GRCh38.p12 chr20: 63,459,050-64,284,202	SOX18, SRMS, 48 more genes
nsv3917244	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 62,125,121-62,363,574 , GRCh37 chr20: 62,654,677-62,893,130 , GRCh38 chr20: 64,023,324-64,261,777	SOX18, MYT1, 10 more genes
nsv3892750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941	SOX18, TGIF2-RAB5IF, 1314 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 53

Page of 3

Number of Variants: 20

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Supplemental Content

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Search details

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