kctd14[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6112766	copy number variation	1	nstd102	human	not provided	GRCh37 chr11: 77,617,820-77,784,237 , GRCh38.p12 chr11: 77,906,774-78,073,191	KCTD14, NDUFC2-KCTD14, 3 more genes
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	KCTD14, FAUP4, 2031 more genes
nsv3921121	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 75,941,754-98,357,960 , NCBI36 chr11: 75,330,446-97,733,898 , GRCh37 chr11: 75,652,798-98,228,688	KCTD14, LOC105369441, 296 more genes
nsv3915804	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,680,927-77,943,941 , NCBI36 chr11: 71,358,575-77,621,589 , GRCh38 chr11: 71,969,881-78,232,895	KCTD14, TPBGL, 173 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	KCTD14, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	KCTD14, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	KCTD14, IGHMBP2, 2829 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	KCTD14, PYGM, 2125 more genes
nsv3898361	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202	KCTD14, SESN3, 694 more genes
nsv3904799	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 77,776,112-77,921,527 , GRCh38.p12 chr11: 78,065,066-78,210,481	NDUFC2, USP35, 7 more genes
nsv6637911	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 77,211,136-78,014,355 , GRCh38.p12 chr11: 77,500,091-78,303,309	KCTD14, RPS20P27, 22 more genes
nsv4455314	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr11: 77,410,575-77,785,783 , GRCh38.p12 chr11: 77,699,530-78,074,737	KCTD14, FTH1P16, 8 more genes
nsv3894547	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 77,415,541-77,785,783 , GRCh38.p12 chr11: 77,704,496-78,074,737	KCTD14, AAMDC, 8 more genes
nsv4729234	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 77,575,261-77,902,589 , GRCh38.p12 chr11: 77,864,215-78,191,543	KCTD14, LOC105369401, 12 more genes

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kctd14[All Fields] AND 1[has_clinical] (15)
dbVar
Concise Conserved Domain Links for Protein (Select 1699430374) (0)
Conserved Domains
txid7234[Organism] (19)
BioProject

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