fam149a[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
nsv3877333	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 187,025,713-187,029,821 , GRCh38.p12 chr4: 186,104,559-186,108,667	FAM149A
nsv3880565	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 187,025,713-187,026,529 , GRCh38.p12 chr4: 186,104,559-186,105,375	FAM149A
nsv3871679	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 187,025,713-187,026,309 , GRCh38.p12 chr4: 186,104,559-186,105,155	FAM149A
nsv3879953	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 187,025,713-187,026,252 , GRCh38.p12 chr4: 186,104,559-186,105,098	FAM149A
nsv3887853	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 187,025,713-187,026,198 , GRCh38.p12 chr4: 186,104,559-186,105,044	FAM149A
nsv3879841	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 187,025,713-187,026,147 , GRCh38.p12 chr4: 186,104,559-186,104,993	FAM149A
nsv3874708	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 187,089,133-187,098,071 , GRCh38.p12 chr4: 186,167,979-186,176,917	FAM149A, LTO1P1
nsv3877879	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 186,983,342-187,054,136 , GRCh38.p12 chr4: 186,062,188-186,132,982	FAM149A, TLR3
nsv3915294	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 187,195,213-187,302,056 , GRCh37.p13 chr4: 186,958,219-187,065,062 , GRCh38.p12 chr4: 186,037,065-186,143,908	FAM149A, TLR3
nsv4682159	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 187,088,122-187,113,191 , GRCh38.p12 chr4: 186,166,968-186,192,037	FAM149A, CYP4V2, 2 more genes
nsv3887695	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 186,953,813-187,201,271 , GRCh38.p12 chr4: 186,032,659-186,280,117	FAM149A, F11, 6 more genes
nsv3913514	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 187,195,284-187,429,742 , GRCh37 chr4: 186,958,290-187,192,748 , GRCh38 chr4: 186,037,136-186,271,594	FAM149A, F11, 6 more genes
nsv6634351	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318	FAM149A, COPS3P1, 363 more genes
nsv4674043	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 165,010,461-190,957,473 , GRCh38.p12 chr4: 164,089,309-190,036,318	FAM149A, CYP4V2, 319 more genes
nsv3912039	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 164,039,530-189,982,708 , GRCh37 chr4: 164,960,682-190,828,225 , NCBI36 chr4: 165,180,132-191,140,857	FAM149A, CYP4V2, 314 more genes
nsv3916579	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 166,202,188-190,939,340 , GRCh38 chr4: 165,281,036-190,018,185 , NCBI36 chr4: 166,421,638-191,176,334	FAM149A, LOC105377614, 291 more genes
nsv4456171	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 166,623,890-190,957,473 , GRCh38.p12 chr4: 165,702,738-190,036,318	FAM149A, TRIML2, 284 more genes
nsv3913994	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 166,317,587-190,095,391 , GRCh37 chr4: 167,238,739-190,828,225 , NCBI36 chr4: 167,458,189-191,250,527	FAM149A, PTGES3P3, 290 more genes
nsv6634364	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 167,779,888-190,957,473 , GRCh38.p12 chr4: 166,858,737-190,036,318	FAM149A, LOC101928551, 279 more genes
nsv3918232	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 168,531,442-191,194,467 , GRCh37 chr4: 168,294,867-190,957,473 , GRCh38 chr4: 167,373,716-190,036,318	FAM149A, LOC105377560, 277 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 149

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Number of Variants: 20

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