elf1[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	ELF1, RNU6-71P, 1332 more genes
nsv3924528	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908	ELF1, LOC105370271, 925 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	ELF1, 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	ELF1, 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	ELF1, 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	ELF1, 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	ELF1, 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	ELF1, 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	ELF1, 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	ELF1, LOC105370170, 100 more genes
nsv3922964	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 10,319,474-13,777,860 , NCBI36 chr19: 10,291,150-13,749,674 , GRCh37 chr19: 10,430,150-13,888,674	SWSAP1, LOC105372284, 164 more genes
nsv3922999	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 10,240,071-12,946,266 , GRCh37.p13 chr19: 10,379,071-13,085,266 , GRCh38.p12 chr19: 10,268,395-12,974,452	ZNF433, MIR6794, 155 more genes
nsv3924466	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 11,496,978-14,126,833 , GRCh38 chr19: 11,525,163-14,155,021 , GRCh37 chr19: 11,635,978-14,265,833	JUNB, ZNF442, 135 more genes
nsv3919036	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 11,628,640-13,336,101 , NCBI36 chr19: 11,489,640-13,197,101 , GRCh38 chr19: 11,517,825-13,225,287	ZNF763, RTBDN, 105 more genes
nsv4729806	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 10,957,601-11,672,041 , GRCh38.p12 chr19: 10,846,925-11,561,226	DOCK6-AS1, C19orf38, 32 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	ELF1, 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	ELF1, 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	ELF1, 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	ELF1, 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	ELF1, RN7SL272P, 1333 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 64

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Number of Variants: 20

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