mtif3[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	MTIF3, RNU6-71P, 1332 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	MTIF3, 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	MTIF3, 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	MTIF3, 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	MTIF3, 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	MTIF3, 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	MTIF3, 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	MTIF3, 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	MTIF3, 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	MTIF3, 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	MTIF3, 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	MTIF3, 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	MTIF3, RNU6-77P, 1317 more genes
nsv3922463	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 18,418,322-114,088,205 , GRCh37 chr13: 19,520,322-115,070,103 , GRCh38 chr13: 18,946,182-114,304,628	MTIF3, TULP3P1, 1311 more genes
nsv6314030	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251	MTIF3, RPSAP53, 1310 more genes
nsv3890649	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,571,503-115,092,569 , GRCh38.p12 chr13: 18,997,363-114,327,094	MTIF3, PPIAP25, 1311 more genes
nsv3906456	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,571,503-115,092,510 , GRCh38.p12 chr13: 18,997,363-114,327,035	MTIF3, HSPD1P9, 1311 more genes
nsv3921223	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 19,671,934-114,340,331 , NCBI36 chr13: 19,144,074-114,123,908 , GRCh37 chr13: 20,246,074-115,085,141	MTIF3, TRIM60P13, 1289 more genes
nsv3916116	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 19,305,270-114,110,683 , GRCh38 chr13: 19,833,130-114,327,106 , GRCh37 chr13: 20,407,270-115,085,141	MTIF3, LOC105370263, 1283 more genes
nsv3917322	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr13: 19,309,535-114,110,750 , GRCh37 chr13: 20,411,535-115,085,141 , GRCh38 chr13: 19,837,395-114,327,173	MTIF3, RNY1P7, 1283 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 33

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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