spata13[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
nsv6313995	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 24,781,425-24,823,602 , GRCh38.p12 chr13: 24,207,287-24,249,464	SPATA13
nsv3910270	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 18,445,862-114,327,173 , NCBI36 chr13: 10,098,739-114,110,750 , GRCh37 chr13: 19,020,001-115,085,141	SPATA13, RNU6-71P, 1332 more genes
nsv4675550	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,436,286-24,970,361 , GRCh38.p12 chr13: 18,862,146-24,396,223	SPATA13, MRPL57, 129 more genes
nsv3890184	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 20,008,480-25,534,121 , GRCh38.p12 chr13: 19,434,340-24,959,983	SPATA13, ANKRD20A19P, 125 more genes
nsv3912021	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 19,144,074-24,458,010 , GRCh38 chr13: 19,671,934-24,985,872 , GRCh37 chr13: 20,246,074-25,560,010	SPATA13, TPTE2P1, 119 more genes
nsv7093994	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 24,293,859-26,594,123 , GRCh38.p12 chr13: 23,719,720-26,019,985	SPATA13, IRX1P1, 54 more genes
nsv3906916	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 23,519,916-24,941,516 , GRCh38.p12 chr13: 22,945,777-24,367,378	SPATA13, SACS-AS1, 29 more genes
nsv3898855	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 23,671,134-24,896,556 , GRCh38.p12 chr13: 23,096,995-24,322,418	SPATA13, MIPEP, 26 more genes
nsv6315495	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403	SPATA13, RNU6-80P, 1334 more genes
nsv6289999	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403	SPATA13, LINC00363, 1334 more genes
nsv3897246	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,031,237-115,107,157 , GRCh38.p12 chr13: 18,457,097-114,341,682	SPATA13, NT5CP3, 1334 more genes
nsv3924676	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 18,456,040-114,340,285 , GRCh37 chr13: 19,030,180-115,105,760 , NCBI36 chr13: 17,928,180-114,123,862	SPATA13, GRTP1, 1334 more genes
nsv5564510	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053	SPATA13, RN7SL272P, 1333 more genes
nsv3894298	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,058,717-115,103,529 , GRCh38.p12 chr13: 18,484,577-114,338,054	SPATA13, DZIP1, 1333 more genes
nsv3916629	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,139,188-115,085,141 , NCBI36 chr13: 18,037,188-114,110,750 , GRCh38 chr13: 18,565,048-114,327,173	SPATA13, TM9SF2, 1330 more genes
nsv6634431	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462	SPATA13, MTUS2-AS1, 1330 more genes
nsv3914899	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,436,286-115,107,733 , GRCh38 chr13: 18,862,146-114,342,258 , NCBI36 chr13: 18,334,286-114,125,835	SPATA13, EFNB2, 1319 more genes
nsv3895329	copy number variation	3	nstd102	human	Pathogenic	GRCh37 chr13: 19,436,286-115,107,733 , GRCh38.p12 chr13: 18,862,146-114,342,258	SPATA13, PPP1R2P10, 1319 more genes
nsv3897712	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr13: 19,436,287-115,107,733 , GRCh38.p12 chr13: 18,862,147-114,342,258	SPATA13, RNU1-24P, 1319 more genes
nsv3919574	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 18,850,545-114,327,173 , GRCh37 chr13: 19,296,527-115,085,141 , NCBI36 chr13: 18,194,527-114,110,750	SPATA13, RNU6-77P, 1317 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 78

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Number of Variants: 20

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