kctd18[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
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	KCTD18, DAZAP2P1, 2991 more genes
nsv3894939	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 175,471,822-204,514,516 , GRCh37 chr2: 175,763,576-204,806,271 , GRCh38 chr2: 174,898,848-203,941,548	KCTD18, TRE-TTC9-1, 412 more genes
nsv6315398	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 185,697,659-213,002,074 , GRCh38.p12 chr2: 184,832,932-212,137,349	KCTD18, LOC107985785, 381 more genes
nsv3899404	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 176,877,419-202,612,758 , GRCh37 chr2: 177,169,173-202,904,513 , GRCh38 chr2: 176,304,445-202,039,790	KCTD18, LINC01877, 326 more genes
nsv3896612	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 192,938,826-215,705,052 , NCBI36 chr2: 193,511,797-216,278,020 , GRCh37 chr2: 193,803,552-216,569,775	KCTD18, MTND4P30, 320 more genes
nsv6637127	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 189,909,904-209,468,383 , GRCh38.p12 chr2: 189,045,178-208,603,658	KCTD18, LOC100421409, 310 more genes
nsv3891560	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 186,027,472-201,059,372 , NCBI36 chr2: 186,600,444-201,632,340 , GRCh37 chr2: 186,892,199-201,924,095	KCTD18, AOX1, 174 more genes
nsv3884912	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 191,750,202-202,297,376 , GRCh38.p12 chr2: 190,885,476-201,432,653	KCTD18, CLK1, 134 more genes
nsv3903696	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 200,510,241-210,604,893 , GRCh37 chr2: 200,801,996-210,896,648 , GRCh38 chr2: 199,937,273-210,031,924	KCTD18, MTND4P23, 206 more genes
nsv3895332	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 200,811,217-210,849,919 , GRCh38 chr2: 199,946,494-209,985,195 , NCBI36 chr2: 200,519,462-210,558,164	KCTD18, CCNYL1, 203 more genes
nsv3881119	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 193,537,927-202,027,736 , GRCh38.p12 chr2: 192,673,201-201,163,013	KCTD18, LOC105376755, 107 more genes
nsv3908231	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 196,233,563-204,542,456 , GRCh38 chr2: 195,660,594-203,969,488 , GRCh37 chr2: 196,525,318-204,834,211	KCTD18, LINC01877, 170 more genes
nsv6313730	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 200,851,079-209,054,267 , GRCh38.p12 chr2: 199,986,356-208,189,543	KCTD18, RN7SKP200, 179 more genes
nsv3876959	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 194,581,315-201,752,422 , GRCh38.p12 chr2: 193,716,591-200,887,699	KCTD18, LOC101927741, 87 more genes
nsv4768322	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 197,359,024-201,383,462 , GRCh38.p12 chr2: 196,494,300-200,518,739	KCTD18, ANKRD44-DT, 48 more genes
nsv4674597	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 201,106,432-204,901,548 , GRCh38.p12 chr2: 200,241,709-204,036,825	KCTD18, KIAA2012-AS1, 113 more genes
nsv3897866	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 198,767,347-202,353,840 , GRCh37 chr2: 199,632,071-203,218,563 , NCBI36 chr2: 199,340,316-202,926,808	KCTD18, RPS2P16, 88 more genes
nsv3892024	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 201,211,431-202,021,140 , NCBI36 chr2: 200,919,676-201,729,385 , GRCh38 chr2: 200,346,708-201,156,417	KCTD18, LOC105373835, 32 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	KCTD18, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	KCTD18, IGKV2OR2-10, 3737 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 37

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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