myo9a[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
nsv3908245	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 72,365,112-72,388,067 , GRCh38.p12 chr15: 72,072,771-72,095,726	MYO9A
nsv3908912	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 72,368,847-72,386,705 , GRCh38.p12 chr15: 72,076,506-72,094,364	MYO9A
nsv3893306	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 72,376,543-72,388,067 , GRCh38.p12 chr15: 72,084,202-72,095,726	MYO9A
nsv3908817	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 72,383,823-72,388,067 , GRCh38.p12 chr15: 72,091,482-72,095,726	MYO9A
nsv3903898	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 72,384,483-72,388,067 , GRCh38.p12 chr15: 72,092,142-72,095,726	MYO9A
nsv3901285	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 72,386,347-72,388,067 , GRCh38.p12 chr15: 72,094,006-72,095,726	MYO9A
nsv3903959	copy number variation	1	nstd102	human	Benign	GRCh37 chr15: 72,386,347-72,386,705 , GRCh38.p12 chr15: 72,094,006-72,094,364	MYO9A
nsv4455666	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,194,247-72,249,034 , GRCh38.p12 chr15: 71,901,906-71,956,693	MYO9A, LOC107984713
nsv3916249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189	MYO9A, H3P40, 1616 more genes
nsv3919468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189	MYO9A, RNU6-18P, 1442 more genes
nsv3913942	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 70,025,300-78,705,993 , NCBI36 chr15: 68,104,693-76,785,390 , GRCh37 chr15: 70,317,639-78,998,335	MYO9A, SNX33, 209 more genes
nsv3920633	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 68,830,574-73,823,337 , NCBI36 chr15: 66,909,967-71,902,731 , GRCh37 chr15: 69,122,913-74,115,678	MYO9A, NEO1, 95 more genes
nsv6309803	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,103,084-74,244,178 , GRCh38.p12 chr15: 71,810,744-73,951,837	MYO9A, PHB1P20, 51 more genes
nsv3900281	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337	MYO9A, MYZAP, 1750 more genes
nsv3913581	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189	MYO9A, MIR4513, 1754 more genes
nsv3904086	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959	MYO9A, TMEM202, 1747 more genes
nsv3905138	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413	MYO9A, FES, 1738 more genes
nsv3892955	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr15: 22,770,422-102,429,112 , GRCh38.p12 chr15: 23,319,714-101,888,909	MYO9A, FAM81A, 1614 more genes
nsv3876912	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 31,115,047-102,354,857 , GRCh38.p12 chr15: 30,822,844-101,814,654	MYO9A, RNU6-953P, 1385 more genes
nsv3899559	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 41,745,084-102,354,798 , GRCh38.p12 chr15: 41,452,886-101,814,595	MYO9A, CILP, 1176 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 34

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Number of Variants: 20

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Supplemental Content

Find related data

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