evi2b[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
nsv5672961	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,422,322-29,665,163 , GRCh38.p12 chr17: 31,095,304-31,338,145	EVI2B, NF1, 3 more genes
nsv5673103	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,422,322-29,664,606 , GRCh38.p12 chr17: 31,095,304-31,337,588	EVI2B, EVI2A, 3 more genes
nsv7094866	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,422,055-29,662,069 , GRCh38.p12 chr17: 31,095,037-31,335,051	EVI2B, EVI2A, 3 more genes
nsv3887599	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,496,889-29,670,173 , GRCh38 chr17: 31,169,871-31,343,155	EVI2B, EVI2A, 3 more genes
nsv5673107	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,527,428-29,657,848 , GRCh38.p12 chr17: 31,200,410-31,330,830	EVI2B, EVI2A, 3 more genes
nsv6289848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,553,499-29,653,041 , GRCh38.p12 chr17: 31,226,481-31,326,023	EVI2B, NF1, 3 more genes
nsv7095093	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,575,982-29,665,843 , GRCh38.p12 chr17: 31,248,964-31,338,825	EVI2B, NF1, 3 more genes
nsv5673111	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,587,625-29,669,475 , GRCh38.p12 chr17: 31,260,607-31,342,457	EVI2B, NF1, 3 more genes
nsv6310161	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,585,342-29,665,843 , GRCh38.p12 chr17: 31,258,324-31,338,825	EVI2B, OMG, 3 more genes
nsv3871300	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,588,729-29,667,663 , GRCh38 chr17: 31,261,711-31,340,645	EVI2B, EVI2A, 3 more genes
nsv5673033	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,587,381-29,662,055 , GRCh38.p12 chr17: 31,260,363-31,335,037	EVI2B, OMG, 3 more genes
nsv5672874	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,592,237-29,653,280 , GRCh38.p12 chr17: 31,265,219-31,326,262	EVI2B, NF1, 3 more genes
nsv1397926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,591,850-29,638,576 , GRCh38 chr17: 31,264,832-31,311,558	EVI2B, NF1, 2 more genes
nsv6309980	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,622,128-29,667,673 , GRCh38.p12 chr17: 31,295,110-31,340,655	EVI2B, OMG, 2 more genes
nsv1398522	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,630,277-29,663,879 , GRCh38 chr17: 31,303,259-31,336,861	EVI2B, EVI2A, 1 more genes
nsv7094968	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,622,027-29,654,877 , GRCh38.p12 chr17: 31,295,009-31,327,859	EVI2B, EVI2A, 2 more genes
nsv7094876	copy number variation	2	nstd102	human	Pathogenic, Likely pathogenic	GRCh37 chr17: 29,585,352-29,670,163 , GRCh38.p12 chr17: 31,258,334-31,343,145	EVI2B, EVI2A, 3 more genes
nsv7095142	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr17: 29,575,982-29,662,069 , GRCh38.p12 chr17: 31,248,964-31,335,051	EVI2B, EVI2A, 3 more genes
nsv5381008	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 29,622,128-29,701,173 , GRCh38.p12 chr17: 31,295,110-31,374,155	EVI2B, OMG, 3 more genes
nsv4683187	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,420,945-29,705,695 , GRCh38.p12 chr17: 31,093,927-31,378,677	EVI2B, AK4P1, 5 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 114

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Number of Variants: 20

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