dusp14[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
nsv4684305	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr17\|NT_187614.1: 1,679,472-1,805,976 , GRCh37 chr17: 35,800,407-35,926,911 , NCBI36 chr17: 32,874,520-33,001,024	DUSP14, SYNRG, 2 more genes
nsv3911811	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577	DUSP14, PRPSAP1, 1350 more genes
nsv1397979	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,360,227-36,473,024 , GRCh38.p12 chr17\|NT_187614.1: 267,755-2,352,089	DUSP14, LOC100420852, 68 more genes
nsv6315528	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,463,923-36,410,559 , GRCh38.p12 chr17\|NT_187614.1: 371,451-2,289,624	DUSP14, LOC105371750, 60 more genes
nsv3894286	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,477,385-36,404,555 , GRCh38.p12 chr17\|NT_187614.1: 384,913-2,283,620	DUSP14, SNORA90, 59 more genes
nsv4684299	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 31,384,281-33,322,972 , GRCh38 chr17\|NT_187614.1: 267,696-2,127,924 , GRCh37 chr17: 34,360,168-36,248,859	DUSP14, DHRS11, 58 more genes
nsv3884569	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 36,143,765-37,995,300 , GRCh37.p13 chr17: 34,900,240-35,888,667	DUSP14, LOC105371749, 54 more genes
nsv3898674	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,447,113-36,283,612 , GRCh38.p12 chr17\|NT_187614.1: 354,641-2,162,677 , GRCh38.p12 chr17: 36,119,723-37,924,067	DUSP14, TBC1D3F, 56 more genes
nsv3907616	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,475,679-36,311,009 , GRCh38.p12 chr17\|NT_187614.1: 383,207-2,190,074	DUSP14, TBC1D3H, 56 more genes
nsv3902415	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,475,679-36,283,612 , GRCh38.p12 chr17: 36,148,298-37,924,067 , GRCh38.p12 chr17\|NT_187614.1: 383,207-2,162,677	DUSP14, LOC105371756, 55 more genes
nsv3916783	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,817,422-36,263,019 , GRCh38 chr17: 36,446,545-38,225,796 , NCBI36 chr17: 31,891,535-33,635,633	DUSP14, ACACA, 50 more genes
nsv3892075	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,450,405-36,248,918 , NCBI36 chr17: 31,474,518-33,323,031 , GRCh38.p12 chr17: 36,123,019-37,889,296 , GRCh38.p12 chr17\|NT_187614.1: 357,933-2,127,983	DUSP14, RPL18AP12, 52 more genes
nsv4684315	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,508,117-36,173,763 , NCBI36 chr17: 31,474,518-33,247,876 , GRCh38 chr17\|NT_187614.1: 357,933-2,052,828	DUSP14, HNF1B, 51 more genes
nsv3904479	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,822,465-36,404,136 , GRCh38.p12 chr17\|NT_187614.1: 701,523-2,283,201	DUSP14, PIGW, 44 more genes
nsv3892538	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 34,822,466-36,404,136 , GRCh38.p12 chr17\|NT_187614.1: 701,524-2,283,201	DUSP14, C17orf78, 44 more genes
nsv3898382	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,822,465-36,397,323 , GRCh38.p12 chr17\|NT_187614.1: 701,523-2,276,388	DUSP14, AATF, 44 more genes
nsv3898201	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,822,465-36,300,630 , GRCh38.p12 chr17\|NT_187614.1: 701,523-2,179,695 , GRCh38.p12 chr17: 36,466,619-38,020,625	DUSP14, RNU6-489P, 45 more genes
nsv3896980	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,822,466-36,300,466 , GRCh38.p12 chr17: 36,466,620-38,020,461 , GRCh38.p12 chr17\|NT_187614.1: 701,524-2,179,531	DUSP14, LOC105371755, 45 more genes
nsv3920659	copy number variation	3	nstd102	human	Pathogenic	GRCh37 chr17: 34,611,352-36,248,918 , NCBI36 chr17: 31,635,465-33,323,031 , GRCh38 chr17: 36,357,258-37,889,296	DUSP14, TADA2A, 40 more genes
nsv3897232	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,822,466-36,351,934 , GRCh38.p12 chr17\|NT_187614.1: 701,524-2,230,999	DUSP14, RPL18AP12, 44 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 113

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Number of Variants: 20

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