foxo1[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
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	FOXO1, RNU6-71P, 1332 more genes
nsv6314117	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618	FOXO1, RBM26, 591 more genes
nsv3915679	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 31,271,865-70,046,105 , GRCh38 chr13: 30,697,728-69,471,973 , NCBI36 chr13: 30,169,865-68,944,106	FOXO1, CCDC70, 524 more genes
nsv3923911	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 38,438,363-68,537,920 , GRCh38 chr13: 37,864,226-67,963,788 , NCBI36 chr13: 37,336,363-67,435,921	FOXO1, MLNR, 422 more genes
nsv3907596	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 32,946,120-62,698,217 , GRCh38.p12 chr13: 32,371,983-62,124,084	FOXO1, TPT1, 434 more genes
nsv3915542	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 37,351,455-63,530,009 , NCBI36 chr13: 36,249,455-62,428,010 , GRCh38 chr13: 36,777,318-62,955,876	FOXO1, LINC02338, 393 more genes
nsv3921404	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 31,592,297-49,065,340 , GRCh38 chr13: 31,018,160-48,491,204 , NCBI36 chr13: 30,490,297-47,963,341	FOXO1, MIR8079, 280 more genes
nsv3923636	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 37,986,314-50,897,351 , GRCh37 chr13: 39,088,314-51,999,350 , GRCh38 chr13: 38,514,177-51,425,214	FOXO1, TUSC8, 251 more genes
nsv3910898	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 34,704,613-40,848,091 , GRCh38 chr13: 35,232,476-41,375,955 , GRCh37 chr13: 35,806,613-41,950,091	FOXO1, LOC105370170, 100 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	FOXO1, 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	FOXO1, 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	FOXO1, 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	FOXO1, 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	FOXO1, 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	FOXO1, 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	FOXO1, 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	FOXO1, 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	FOXO1, 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	FOXO1, 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	FOXO1, RNU1-24P, 1319 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 41

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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