ccr9[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
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	CCR9, TMEM89, 129 more genes
nsv3881275	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 41,104,508-44,636,698 , GRCh38.p12 chr3: 41,063,017-44,595,206	LOC107986077, LOC105377052, 69 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	CCR9, 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	CCR9, 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	CCR9, 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	RNU6-243P, ZNF385D, 382 more genes
nsv4347762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589	CCR9, UQCRC1, 291 more genes
nsv3921797	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 45,896,379-50,762,357 , GRCh38 chr3: 45,879,883-50,749,922 , GRCh37 chr3: 45,921,375-50,787,353	CCR9, RBM5-AS1, 185 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	CCR9, ACAA1, 344 more genes
nsv3912340	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr3: 45,733,423-46,319,401 , GRCh38 chr3: 45,691,931-46,277,910 , NCBI36 chr3: 45,708,427-46,294,405	CCR9, LOC105377063, 14 more genes
nsv4451167	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 45,862,803-46,173,511 , GRCh38.p12 chr3: 45,821,311-46,132,019	CCR9, NRBF2P2, 7 more genes
nsv4683137	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 45,867,806-46,063,439 , GRCh38.p12 chr3: 45,826,314-46,021,947	CCR9, CXCR6, 6 more genes
nsv7096805	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 45,435,946-49,137,751 , GRCh38.p12 chr3: 45,394,454-49,100,318	CCR9, SNORA94, 120 more genes
nsv6311795	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 40,924,962-43,760,024 , GRCh38.p12 chr3: 40,883,471-43,718,532	VIPR1, SNRK-AS1, 52 more genes

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