dbVar for OMIM (Select 613113) - 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
nsv7098692	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 31,155,962-31,163,396 , GRCh37.p13 chr17: 29,482,980-29,490,414	NF1
nsv7095328	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,663,341-29,679,442 , GRCh38.p12 chr17: 31,336,323-31,352,424	NF1, AK4P1
nsv7095327	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,654,575-29,667,842 , GRCh38.p12 chr17: 31,327,557-31,340,824	NF1
nsv7095144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,676,118-29,687,741 , GRCh38.p12 chr17: 31,349,100-31,360,723	NF1
nsv7095143	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,585,352-29,592,367 , GRCh38.p12 chr17: 31,258,334-31,265,349	NF1
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	EVI2A, EVI2B, 3 more genes
nsv7095141	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,475,515-29,542,762 , GRCh38.p12 chr17: 31,148,497-31,215,744	NF1
nsv7095140	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr17: 29,475,515-29,490,414 , GRCh38.p12 chr17: 31,148,497-31,163,396	NF1
nsv7095139	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 29,422,055-29,552,288 , GRCh38.p12 chr17: 31,095,037-31,225,270	NF1
nsv7095094	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,592,237-29,701,173 , GRCh38.p12 chr17: 31,265,219-31,374,155	AK4P1, EVI2A, 4 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	NF1, LOC101927057, 3 more genes
nsv7095092	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,557,258-29,563,059 , GRCh38.p12 chr17: 31,230,240-31,236,041	NF1
nsv7095091	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr17: 29,556,023-29,563,059 , GRCh38.p12 chr17: 31,229,005-31,236,041	NF1
nsv7095090	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,527,428-29,592,367 , GRCh38.p12 chr17: 31,200,410-31,265,349	NF1
nsv7095089	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,527,420-29,701,173 , GRCh38.p12 chr17: 31,200,402-31,374,155	AK4P1, EVI2A, 4 more genes
nsv7095088	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,422,328-29,677,356 , GRCh38.p12 chr17: 31,095,310-31,350,338	AK4P1, EVI2A, 4 more genes
nsv7095087	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,422,055-29,422,407 , GRCh38.p12 chr17: 31,095,037-31,095,389	NF1
nsv7095086	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 27,573,882-29,576,157 , GRCh38.p12 chr17: 29,246,864-31,249,139	LOC107984990, ADAP2, 59 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	EVI2A, EVI2B, 2 more genes
nsv7094967	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 29,559,879-29,685,283 , GRCh38.p12 chr17: 31,232,861-31,358,265	AK4P1, EVI2A, 4 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

Links from OMIM

Items: 1 to 20 of 282

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Number of Variants: 20

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