ttc23[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
nsv3904353	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 99,722,841-99,760,335 , GRCh38.p12 chr15: 99,182,636-99,220,130	TTC23
nsv6637460	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 99,722,842-99,760,335 , GRCh38.p12 chr15: 99,182,637-99,220,130	TTC23
nsv6291706	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 99,722,958-99,760,335 , GRCh38.p12 chr15: 99,182,753-99,220,130	TTC23
nsv3899179	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 99,521,882-99,778,744 , GRCh38.p12 chr15: 98,978,653-99,238,539	TTC23, LUNAR1, 3 more genes
nsv4675426	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 99,636,901-99,762,146 , GRCh38.p12 chr15: 99,096,698-99,221,941	TTC23, SYNM, 1 more genes
nsv6637398	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 99,744,524-99,847,122 , GRCh38.p12 chr15: 99,204,319-99,306,917	TTC23, LRRC28, 2 more genes
nsv6638014	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 99,521,882-99,706,878 , GRCh38.p12 chr15: 98,978,653-99,166,673	TTC23, LUNAR1, 3 more genes
nsv3914508	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 97,253,459-97,540,481 , GRCh37 chr15: 99,435,936-99,722,958 , GRCh38 chr15: 98,892,707-99,182,753	TTC23, IGF1R, 4 more genes
nsv6313947	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 99,439,498-99,720,434 , GRCh38.p12 chr15: 98,896,269-99,180,229	TTC23, IGF1R, 4 more genes
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	TTC23, 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	TTC23, RNU6-18P, 1442 more genes
nsv4729092	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189	TTC23, CHD2, 272 more genes
nsv4675149	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909	TTC23, TTLL13, 264 more genes
nsv3908429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 90,346,994-102,354,798 , GRCh38.p12 chr15: 89,803,763-101,814,595	TTC23, RPL31P55, 201 more genes
nsv3899918	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 92,197,136-102,354,857 , GRCh38.p12 chr15: 91,653,906-101,814,654	TTC23, SNRPCP18, 148 more genes
nsv6112780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538	TTC23, LOC105371009, 149 more genes
nsv3919064	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 91,542,950-100,200,996 , GRCh38 chr15: 93,198,717-101,843,270 , GRCh37 chr15: 93,741,946-102,383,473	TTC23, LOC105371032, 126 more genes
nsv3918825	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 94,348,261-101,867,081 , GRCh38 chr15: 93,805,032-101,326,876 , NCBI36 chr15: 92,149,265-99,684,604	TTC23, LOC440311, 107 more genes
nsv3922914	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 92,814,458-100,338,915 , GRCh37.p13 chr15: 95,013,454-102,521,392 , GRCh38.p12 chr15: 94,470,225-101,981,189	TTC23, OR4F14P, 124 more genes
nsv3897684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 95,136,822-102,045,577 , GRCh38.p12 chr15: 94,593,593-101,505,374	TTC23, ARRDC4, 98 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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