tenm3[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
nsv3888862	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 183,570,100-183,572,390 , GRCh38.p12 chr4: 182,648,947-182,651,237	TENM3
nsv3887303	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 183,570,571-183,572,390 , GRCh38.p12 chr4: 182,649,418-182,651,237	TENM3
nsv3885790	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr4: 183,214,583-183,488,926 , GRCh38.p12 chr4: 182,293,430-182,567,773	TENM3, RNU2-34P
nsv3888285	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 183,689,629-183,750,550 , GRCh38.p12 chr4: 182,768,476-182,829,397	TENM3, LOC105377571
nsv3921752	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr4: 182,793,418-182,892,852 , NCBI36 chr4: 183,951,565-184,050,999 , GRCh37 chr4: 183,714,571-183,814,005	TENM3, LOC105377576, 1 more genes
nsv3915560	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr4: 181,078,045-181,624,596 , GRCh37 chr4: 181,999,198-182,545,749 , NCBI36 chr4: 182,236,192-182,782,743	TENM3, LINC02500, 3 more genes
nsv3873534	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 183,259,550-183,613,837 , GRCh38.p12 chr4: 182,338,397-182,692,684	TENM3, RN7SKP67, 1 more genes
nsv4455743	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 183,686,417-183,836,339 , GRCh38.p12 chr4: 182,765,264-182,915,186	TENM3, LOC105377571, 2 more genes
nsv4455184	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 183,686,417-183,832,624 , GRCh38.p12 chr4: 182,765,264-182,911,471	TENM3, LOC105377576, 2 more genes
nsv3915054	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 183,914,353-184,050,968 , GRCh37.p13 chr4: 183,677,359-183,813,974 , GRCh38.p12 chr4: 182,756,206-182,892,821	TENM3, LOC105377576, 2 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	TENM3, 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	TENM3, 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	TENM3, 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	TENM3, 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	TENM3, 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	TENM3, 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	TENM3, 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	TENM3, LOC105377560, 277 more genes
nsv3882557	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 169,969,014-190,957,473 , GRCh38.p12 chr4: 169,047,863-190,036,318	TENM3, LOC105377530, 258 more genes
nsv3921438	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 169,873,508-190,018,185 , NCBI36 chr4: 171,031,234-191,176,334 , GRCh37 chr4: 170,794,659-190,939,340	TENM3, FAUP3, 245 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 118

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Number of Variants: 20

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