clec3b[All Fields] AND 1[has_clinical] - dbVar

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Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6315166	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 44,948,482-49,115,809 , GRCh38.p12 chr3: 44,906,990-49,078,376	CLEC3B, TMEM89, 129 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	CLEC3B, 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	CLEC3B, 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	CLEC3B, RPL23AP49, 2875 more genes
nsv3885169	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 16,923,595-45,249,923 , GRCh38.p12 chr3: 16,884,818-45,208,431	CLEC3B, RNU6-243P, 382 more genes
nsv3883164	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 37,028,313-49,929,220 , GRCh38.p12 chr3: 36,986,822-49,891,787	CLEC3B, ACAA1, 344 more genes
nsv4674744	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 44,444,902-45,413,927 , GRCh38.p12 chr3: 44,403,410-45,372,435	CLEC3B, RPL12P44, 37 more genes
nsv3921567	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 45,050,227-45,247,771 , GRCh37.p13 chr3: 45,075,223-45,272,767 , GRCh38.p12 chr3: 45,033,731-45,231,275	CLEC3B, CDCP1, 4 more genes

dbVar