srxn1[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
nsv3912645	copy number variation	1	nstd102	human	Benign	GRCh38 chr20: 590,507-661,733 , GRCh37 chr20: 571,151-642,377 , NCBI36 chr20: 519,151-590,377	SRXN1, TCF15, 2 more genes
nsv3924828	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr20: 519,151-607,871 , GRCh37 chr20: 571,151-659,871 , GRCh38 chr20: 590,507-679,227	SRXN1, LOC107985423, 2 more genes
nsv6315567	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 453,176-822,262 , GRCh37.p13 chr20: 433,820-802,905	SRXN1, CSNK2A1, 5 more genes
nsv6311232	copy number variation	3	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr20: 389,402-746,418 , GRCh38.p12 chr20: 408,758-765,774	SRXN1, CSNK2A1, 6 more genes
nsv4676270	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,568-2,269,777 , GRCh38.p12 chr20: 80,927-2,289,131	SRXN1, LOC100289473, 60 more genes
nsv3917810	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 121,781-2,290,194 , GRCh37 chr20: 102,422-2,270,840 , NCBI36 chr20: 50,422-2,218,840	SRXN1, RAD21L1, 59 more genes
nsv1398608	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 71,023-2,129,746 , GRCh38.p12 chr20: 90,382-2,149,100	SRXN1, SIRPB3P, 58 more genes
nsv3899121	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 121,521-2,073,612 , GRCh38.p12 chr20: 140,880-2,092,966	SRXN1, RN7SL561P, 56 more genes
nsv3914701	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 70,580-1,919,864 , NCBI36 chr20: 18,580-1,867,864 , GRCh38 chr20: 89,939-1,939,218	SRXN1, MIR6869, 54 more genes
nsv3916212	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr20: 18,580-1,781,123 , GRCh37 chr20: 70,580-1,833,123 , GRCh38 chr20: 89,939-1,852,477	SRXN1, NRSN2-AS1, 52 more genes
nsv3907056	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,568-1,823,540 , GRCh38.p12 chr20: 80,927-1,842,894	SRXN1, ACTG1P3, 52 more genes
nsv3923563	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 18,580-1,699,213 , GRCh37 chr20: 70,580-1,751,213 , GRCh38 chr20: 89,939-1,770,567	SRXN1, LOC101929937, 50 more genes
nsv3924759	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 18,580-1,422,759 , GRCh38 chr20: 89,939-1,494,113 , GRCh37 chr20: 70,580-1,474,759	SRXN1, DEFB127, 39 more genes
nsv3915146	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 18,580-1,288,754 , GRCh38 chr20: 89,939-1,360,110 , GRCh37 chr20: 70,580-1,340,754	SRXN1, TMEM74B, 34 more genes
nsv4676288	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 61,568-1,305,971 , GRCh38.p12 chr20: 80,927-1,325,327	SRXN1, TBC1D20, 34 more genes
nsv3914263	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 80,093-1,246,766 , NCBI36 chr20: 8,734-1,175,410 , GRCh37 chr20: 60,734-1,227,410	SRXN1, TBC1D20, 30 more genes
nsv5381806	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 67,778-974,841 , GRCh38.p12 chr20: 87,137-994,198	SRXN1, DEFB132, 24 more genes
nsv3914223	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 89,939-975,656 , GRCh37 chr20: 70,580-956,299 , NCBI36 chr20: 18,580-904,299	SRXN1, DEFB125, 24 more genes
nsv4684288	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-813,880 , GRCh38.p12 chr20: 82,603-833,237	SRXN1, DEFB129, 20 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	SRXN1, 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 63

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Number of Variants: 20

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