medag[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
nsv4674853	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 31,498,706-31,566,543 , GRCh38.p12 chr13: 30,924,569-30,992,406	MEDAG, TEX26, 2 more genes
nsv6637215	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 31,267,070-31,483,281 , GRCh38.p12 chr13: 30,692,933-30,909,144	MEDAG, LINC00398, 3 more genes
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	MEDAG, RNU6-71P, 1332 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	MEDAG, CCDC70, 524 more genes
nsv3924246	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 29,785,946-38,739,818 , GRCh37 chr13: 30,887,946-39,841,818 , GRCh38 chr13: 30,313,809-39,267,681	MEDAG, LINC01048, 117 more genes
nsv3920559	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 29,647,457-37,130,151 , NCBI36 chr13: 28,545,457-36,028,151 , GRCh38 chr13: 29,073,320-36,556,014	MEDAG, LINC02343, 92 more genes
nsv6112810	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 28,925,153-34,061,696 , GRCh38.p12 chr13: 28,351,016-33,487,559	MEDAG, MTUS2, 70 more genes
nsv3923402	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 30,228,271-33,432,383 , GRCh38 chr13: 29,654,134-32,858,245 , NCBI36 chr13: 29,126,271-32,330,383	MEDAG, RXFP2, 53 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	MEDAG, 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	MEDAG, 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	MEDAG, 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	MEDAG, 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	MEDAG, 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	MEDAG, 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	MEDAG, 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	MEDAG, 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	MEDAG, 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	MEDAG, 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	MEDAG, 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	MEDAG, 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 39

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Number of Variants: 20

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Supplemental Content

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