myo16[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
nsv6314478	complex chromosomal rearrangement	3	nstd102	human	Pathogenic	GRCh38.p12 chr13: 101,317,547-101,317,547 , GRCh38.p12 chr13: 101,321,256-101,321,256 , GRCh38.p12 chr13: 108,561,681-108,561,681 , GRCh38.p12 chr13: 108,561,710-108,561,710 , GRCh37 chr13: 109,214,029-109,214,029 , GRCh37 chr13: 109,214,058-109,214,058 , GRCh37 chr13: 101,969,898-101,969,898 , GRCh37 chr13: 101,973,607-101,973,607 , GRCh37 chr7: 49,277,729-49,277,729 , GRCh37 chr7: 49,277,887-49,277,887 , GRCh38.p12 chr7: 49,238,133-49,238,133 , GRCh38.p12 chr7: 49,238,291-49,238,291	MYO16, NALCN
nsv3909140	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr13: 109,048,333-109,543,096 , GRCh38.p12 chr13: 108,395,985-108,890,748	MYO16, HCFC2P1
nsv3908007	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 109,686,709-109,969,952 , GRCh38.p12 chr13: 109,034,361-109,317,604	MYO16, MYO16-AS1, 1 more genes
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	MYO16, 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	MYO16, LOC105370271, 925 more genes
nsv4675850	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258	MYO16, TEX30, 680 more genes
nsv3907697	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 53,551,300-109,850,651 , GRCh38.p12 chr13: 52,977,165-109,198,303	MYO16, GPC5, 565 more genes
nsv6314171	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 79,370,012-115,107,733 , GRCh38.p12 chr13: 78,795,877-114,342,258	MYO16, MIR4705, 430 more genes
nsv3920102	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 86,788,927-114,340,331 , GRCh37 chr13: 87,441,182-115,085,141 , NCBI36 chr13: 86,239,183-114,123,908	MYO16, LOC107984609, 369 more genes
nsv3903376	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 88,073,140-115,107,733 , GRCh38.p12 chr13: 87,420,885-114,342,258	MYO16, ZIC2, 364 more genes
nsv3896487	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 89,796,110-115,083,342 , GRCh38.p12 chr13: 89,143,856-114,317,867	MYO16, TMTC4, 347 more genes
nsv3890560	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 94,474,530-115,107,733 , GRCh38.p12 chr13: 93,822,277-114,342,258	MYO16, RPL15P18, 303 more genes
nsv3892450	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 96,586,481-115,107,733 , GRCh38.p12 chr13: 95,934,227-114,342,258	MYO16, RPS6P23, 268 more genes
nsv4675644	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 96,895,656-115,107,733 , GRCh38.p12 chr13: 96,243,402-114,342,258	MYO16, ZIC2, 266 more genes
nsv6637400	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 97,142,120-115,107,733 , GRCh38.p12 chr13: 96,489,866-114,342,258	MYO16, LOC107984609, 265 more genes
nsv5672796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 94,679,977-111,536,145 , GRCh38.p12 chr13: 94,027,723-110,883,798	MYO16, LINC00359, 220 more genes
nsv3914527	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 93,345,058-109,458,154 , NCBI36 chr13: 92,795,312-108,908,502 , GRCh37 chr13: 93,997,311-110,110,501	MYO16, DOCK9, 196 more genes
nsv3904662	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 94,703,767-109,731,879 , GRCh38.p12 chr13: 94,051,513-109,079,531	MYO16, LOC107984615, 189 more genes
nsv6314066	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 100,258,328-115,107,733 , GRCh38.p12 chr13: 99,606,074-114,342,258	MYO16, MIR4502, 208 more genes
nsv3905010	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 101,075,864-115,105,020 , GRCh38.p12 chr13: 100,423,610-114,339,545	MYO16, RN7SKP10, 194 more genes

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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 116

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Number of Variants: 20

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