eif5a[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
nsv3910581	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr10: 80,851,761-80,955,586 , GRCh37.p13 chr10: 81,181,755-81,285,580 , GRCh38.p12 chr10: 79,421,999-79,525,824	TPRX1P1, ZCCHC24, 3 more genes
nsv4682723	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 80,961,390-81,319,734 , GRCh38.p12 chr10: 79,201,633-79,559,978	PPIF, ZMIZ1, 7 more genes
nsv7137209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639	RNU7-12P, RNU1-65P, 1876 more genes
nsv3913013	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 162,016-7,697,012 , GRCh37 chr17: 45,835-7,600,330 , NCBI36 chr17: 11,807-7,541,055	EIF5A, RPS4XP17, 289 more genes
nsv3910343	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 5,636,297-7,942,140 , NCBI36 chr17: 5,577,021-7,882,865 , GRCh38 chr17: 5,732,977-8,038,822	EIF5A, RPL23AP73, 106 more genes
nsv1397967	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 6,838,295-7,991,364 , GRCh37.p13 chr17: 6,897,571-8,050,639 , GRCh38.p12 chr17: 6,994,252-8,147,321	EIF5A, TNFSF12-TNFSF13, 96 more genes
nsv7095414	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,123,304-8,193,254 , GRCh38.p12 chr17: 7,219,985-8,289,936	EIF5A, CTC1, 103 more genes
nsv6314103	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,020,054-8,086,290 , GRCh38.p12 chr17: 7,116,735-8,182,972	EIF5A, RPL7AP64, 87 more genes
nsv7094915	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,120,455-8,151,423 , GRCh38.p12 chr17: 7,217,136-8,248,105	EIF5A, MIR324, 101 more genes
nsv1398205	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 7,033,635-7,977,678 , GRCh37.p13 chr17: 7,092,911-8,036,953 , GRCh38.p12 chr17: 7,189,592-8,133,635	EIF5A, YBX2, 76 more genes
nsv7098895	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,004,894-7,766,789 , GRCh38.p12 chr17: 7,101,575-7,863,471	EIF5A, LOC105371512, 61 more genes
nsv4676022	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 6,800,893-7,304,696 , GRCh38.p12 chr17: 6,897,574-7,401,377	EIF5A, DVL2, 37 more genes
nsv3922376	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 7,210,345-7,496,934 , NCBI36 chr17: 7,054,388-7,340,977 , GRCh37 chr17: 7,113,664-7,400,253	EIF5A, DVL2, 29 more genes
nsv4729957	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,014,481-7,283,233 , GRCh38.p12 chr17: 7,111,162-7,379,914	EIF5A, MIR324, 20 more genes
nsv1398520	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 6,936,148-7,177,360 , GRCh37.p13 chr17: 6,995,424-7,236,636 , GRCh38.p12 chr17: 7,092,105-7,333,317	EIF5A, ELP5, 16 more genes
nsv1398446	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 6,996,378-7,152,828 , GRCh37.p13 chr17: 7,055,654-7,212,104 , GRCh38.p12 chr17: 7,152,335-7,308,785	EIF5A, ASGR1, 11 more genes
nsv3906389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996	LOC100419870, LOC102724439, 2105 more genes
nsv3891157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558	AGAP14P, LOC100505502, 2097 more genes
nsv3902271	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639	ANXA11, EDRF1-DT, 2085 more genes
nsv3891958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414	TUBB8, PPP2R2D, 2085 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 52

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Number of Variants: 20

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