mylk4[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6290973	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr6: 2,370,075-2,688,038 , GRCh38.p12 chr6: 2,369,841-2,687,804	MYLK4, LINC02521, 2 more genes
nsv3911792	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 101,974-13,964,135 , GRCh38 chr6: 156,974-13,855,925 , GRCh37 chr6: 156,974-13,856,156	MYLK4, SIRT5, 228 more genes
nsv3873362	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 204,009-11,608,587 , GRCh38.p12 chr6: 204,009-11,608,354	MYLK4, LOC100506207, 193 more genes
nsv3923249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 110,675-8,981,266 , GRCh38 chr6: 165,675-9,036,034 , GRCh37 chr6: 165,675-9,036,267	MYLK4, LOC100506207, 148 more genes
nsv3916436	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 156,974-7,122,992 , NCBI36 chr6: 101,974-7,067,991 , GRCh38 chr6: 156,974-7,122,759	MYLK4, LINC01011, 119 more genes
nsv3883703	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 156,974-6,417,749 , GRCh38.p12 chr6: 156,974-6,417,516	MYLK4, LOC107986514, 108 more genes
nsv3875400	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 204,009-6,447,311 , GRCh38.p12 chr6: 204,009-6,447,078	MYLK4, FAM217A, 107 more genes
nsv3914400	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 97,634-6,235,036 , GRCh38 chr6: 152,634-6,289,804 , GRCh37 chr6: 152,634-6,290,037	MYLK4, LOC105374898, 106 more genes
nsv3922576	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 164,633-6,284,470 , GRCh38 chr6: 164,633-6,284,237 , NCBI36 chr6: 109,633-6,229,469	MYLK4, GLRX3P2, 106 more genes
nsv3914814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 163,083-6,063,033 , GRCh38 chr6: 163,083-6,062,800 , NCBI36 chr6: 108,083-6,008,032	MYLK4, LINC02521, 103 more genes
nsv3912779	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 163,083-5,875,635 , GRCh38 chr6: 163,083-5,875,402 , NCBI36 chr6: 108,083-5,820,634	MYLK4, ECI2, 98 more genes
nsv3920236	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 164,633-5,823,834 , GRCh38 chr6: 164,633-5,823,601 , NCBI36 chr6: 109,633-5,768,833	MYLK4, TUBB2A, 98 more genes
nsv3915132	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 152,634-5,315,912 , GRCh38 chr6: 152,634-5,315,679 , NCBI36 chr6: 97,634-5,260,911	MYLK4, LOC101927888, 94 more genes
nsv3910975	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 107,682-4,979,015 , NCBI36 chr6: 52,682-4,924,014 , GRCh38 chr6: 107,682-4,978,781	MYLK4, RNA5SP201, 90 more genes
nsv3916403	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 156,974-4,907,692 , GRCh37 chr6: 156,974-4,907,926 , NCBI36 chr6: 101,974-4,852,925	MYLK4, MIR6720, 86 more genes
nsv3877391	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 2,109,893-5,962,832 , GRCh38.p12 chr6: 2,109,659-5,962,599	MYLK4, LOC107986516, 76 more genes
nsv3882883	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 383,951-4,183,288 , GRCh38.p12 chr6: 383,951-4,183,054	MYLK4, TUBB2BP1, 69 more genes
nsv6636564	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-3,718,881 , GRCh38.p12 chr6: 156,975-3,718,647	MYLK4, LOC101927691, 60 more genes
nsv6313679	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 383,951-3,898,619 , GRCh38.p12 chr6: 383,951-3,898,385	MYLK4, SERPINB9P1, 59 more genes
nsv7137049	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 393,153-3,751,765 , GRCh38.p12 chr6: 393,153-3,751,531	MYLK4, LOC105374883, 57 more genes

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

Send to:

Search results

Items: 1 to 20 of 61

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

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 61

Page of 4

Number of Variants: 20

Page of 4

Supplemental Content

Find related data

Search details

Recent activity