kbtbd8[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3916461	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 57,174,452-90,309,110 , NCBI36 chr3: 57,149,492-90,391,800 , GRCh38 chr3: 57,140,424-90,259,960	KBTBD8, LOC105377171, 323 more genes
nsv3922768	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 64,746,924-78,459,248 , GRCh38 chr3: 64,761,248-78,410,098 , NCBI36 chr3: 64,721,964-78,541,938	KBTBD8, RNU6-557P, 147 more genes
nsv6290933	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 59,332,508-70,686,155 , GRCh38.p12 chr3: 59,346,782-70,637,004	KBTBD8, NDUFB4P1, 110 more genes
nsv3883532	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 66,133,719-75,076,440 , GRCh38.p12 chr3: 66,148,044-75,027,289	KBTBD8, PSMD12P1, 93 more genes
nsv3922383	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,956,521-68,514,983 , NCBI36 chr3: 61,931,561-68,597,673 , GRCh38 chr3: 61,970,847-68,465,832	KBTBD8, UBL5P3, 73 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	KBTBD8, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	KBTBD8, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	KBTBD8, RPL23AP49, 2875 more genes
nsv3871428	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 65,448,161-67,286,083 , GRCh38.p12 chr3: 65,462,486-67,235,659	KBTBD8, LOC105377141, 19 more genes
nsv6636503	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 65,448,162-67,283,742 , GRCh38.p12 chr3: 65,462,487-67,233,318	KBTBD8, RN7SL482P, 19 more genes
nsv4674691	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 65,459,431-67,283,891 , GRCh38.p12 chr3: 65,473,756-67,233,467	KBTBD8, SLC25A26, 19 more genes
nsv3920642	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 65,470,758-67,269,091 , NCBI36 chr3: 65,445,798-67,351,781 , GRCh38 chr3: 65,485,083-67,218,667	KBTBD8, MAGI1-AS1, 18 more genes

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