ckmt1b[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
nsv4684065	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 43,891,870-43,910,920 , GRCh38.p12 chr15: 43,599,672-43,618,722	CKMT1B, RNU6-554P, 1 more genes
nsv1398238	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 43,891,870-43,910,920 , GRCh38 chr15: 43,599,672-43,618,722	CKMT1B, STRC, 1 more genes
nsv3879437	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 43,599,438-43,613,711 , GRCh37.p13 chr15: 43,891,636-43,905,909	CKMT1B, STRC, 1 more genes
nsv6290550	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr15: 43,891,870-43,901,474 , GRCh38 chr15: 43,599,672-43,609,276	CKMT1B, STRC, 1 more genes
nsv7137025	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr15: 43,891,760-43,900,060 , GRCh38.p12 chr15: 43,599,562-43,607,862	CKMT1B, STRC, 1 more genes
nsv3880040	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 43,891,870-43,897,597 , GRCh38 chr15: 43,599,672-43,605,399	CKMT1B, STRC, 1 more genes
nsv6290205	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 43,851,199-43,924,279 , GRCh38.p12 chr15: 43,559,001-43,632,081	CKMT1B, PPIP5K1, 4 more genes
nsv3913560	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 41,676,219-41,738,593 , GRCh37 chr15: 43,888,927-43,951,301 , GRCh38 chr15: 43,596,729-43,659,103	CKMT1B, CATSPER2, 5 more genes
nsv7093388	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 43,888,606-43,941,032 , GRCh38.p12 chr15: 43,596,408-43,648,834	CKMT1B, CATSPER2, 5 more genes
nsv4350148	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 43,890,409-43,939,642 , GRCh38.p12 chr15: 43,598,211-43,647,444	CKMT1B, CATSPER2, 5 more genes
nsv3873114	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 43,890,409-43,939,642 , GRCh38.p12 chr15: 43,598,211-43,647,444	CKMT1B, CATSPER2, 5 more genes
nsv4348765	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 43,891,364-43,939,659 , GRCh38.p12 chr15: 43,599,166-43,647,461	CKMT1B, CATSPER2, 5 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	CKMT1B, 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	CKMT1B, RNU6-18P, 1442 more genes
nsv3903255	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 41,689,327-52,446,981 , GRCh38.p12 chr15: 41,397,129-52,154,784	CKMT1B, RN7SKP101, 234 more genes
nsv3903669	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 43,759,773-53,252,240 , GRCh38.p12 chr15: 43,467,575-52,960,043	CKMT1B, MIR4712, 188 more genes
nsv3902367	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 42,850,434-49,592,633 , GRCh38.p12 chr15: 42,558,236-49,300,436	CKMT1B, SERF2-C15ORF63, 142 more genes
nsv6290201	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 43,851,199-44,038,820 , GRCh38.p12 chr15: 43,559,001-43,746,622	CKMT1B, CATSPER2P1, 13 more genes
nsv6290131	copy number variation	2	nstd102	human	Pathogenic, Likely pathogenic	GRCh37 chr15: 43,851,199-44,038,794 , GRCh38.p12 chr15: 43,559,001-43,746,596	CKMT1B, STRCP1, 13 more genes
nsv3906590	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 43,868,571-44,014,518 , GRCh38.p12 chr15: 43,576,373-43,722,320	CKMT1B, PPIP5K1P1-CATSPER2, 10 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 68

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Number of Variants: 20

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