ccdc18[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 9

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Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3872091	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 93,667,456-93,741,025 , GRCh38.p12 chr1: 93,201,899-93,275,468	CCDC18, LOC107985521
nsv4768351	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 92,405,898-94,018,197 , GRCh38.p12 chr1: 91,940,341-93,552,640	CCDC18, MND1P1, 39 more genes
nsv3899032	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 92,729,074-93,745,436 , GRCh38 chr1: 92,490,929-93,507,291 , GRCh37 chr1: 92,956,486-93,972,848	CCDC18, EVI5, 24 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	CCDC18, MARK1, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	CCDC18, SNAP47, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	CCDC18, RNU1-153P, 4887 more genes
nsv3898327	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 83,457,325-104,273,917 , GRCh37 chr1: 83,923,008-104,816,539 , NCBI36 chr1: 83,695,596-104,618,062	CCDC18, LINC01773, 322 more genes
nsv3883510	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 93,603,954-93,827,300 , GRCh38.p12 chr1: 93,138,397-93,361,743	CCDC18, TMED5, 6 more genes
nsv4436181	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532	CCDC18, LINC01776, 1853 more genes

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