mov10[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6313675	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309	MOV10, LINC01307, 320 more genes
nsv5381058	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 102,021,465-119,737,478 , GRCh38.p12 chr1: 101,555,909-119,194,855	MOV10, AMYP1, 320 more genes
nsv7095695	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 111,145,905-114,454,813 , GRCh38.p12 chr1: 110,603,283-113,912,191	MOV10, LOC107985189, 83 more genes
nsv7095696	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 112,318,699-115,576,848 , GRCh38.p12 chr1: 111,776,077-115,034,227	MOV10, AKR7A2P1, 69 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	MOV10, 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	MOV10, 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	MOV10, RNU1-153P, 4887 more genes
nsv3882464	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 93,837,992-121,343,783 , GRCh38.p12 chr1: 93,372,435-121,601,985	MOV10, LINC02607, 513 more genes
nsv3890331	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 104,669,629-120,321,801 , GRCh37 chr1: 104,868,106-120,471,049 , GRCh38 chr1: 104,325,484-119,977,655	MOV10, OR11I1P, 324 more genes
nsv6313671	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 111,647,582-121,343,783 , GRCh38.p12 chr1: 111,104,960-121,601,985	MOV10, GAPDHP23, 243 more genes
nsv3898188	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 110,100,775-118,994,350 , GRCh38 chr1: 109,756,630-118,650,204 , GRCh37 chr1: 110,299,252-119,192,827	MOV10, AP4B1-AS1, 198 more genes
nsv3889261	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 113,186,778-113,373,705 , GRCh38.p12 chr1: 112,644,156-112,831,083	MOV10, RHOC, 6 more genes
nsv3897628	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr1: 112,625,023-113,046,966 , NCBI36 chr1: 112,969,168-113,391,111 , GRCh37 chr1: 113,167,645-113,589,588	MOV10, LOC105378911, 17 more genes
nsv1398301	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 113,134,186-113,265,713 , GRCh38.p12 chr1: 112,591,564-112,723,091	MOV10, ST7L, 7 more genes
nsv3894232	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr1: 112,491,547-113,814,203 , GRCh37 chr1: 112,690,024-114,012,680 , GRCh38 chr1: 112,147,402-113,470,058	MOV10, LOC100421402, 30 more genes
nsv3889062	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 113,213,652-113,947,403 , GRCh38.p12 chr1: 112,671,030-113,404,781	MOV10, LINC01356, 21 more genes
nsv3900976	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr1: 113,031,469-113,560,603 , GRCh38 chr1: 112,687,324-113,216,458 , GRCh37 chr1: 113,229,946-113,759,080	MOV10, SLC16A1, 19 more genes
nsv4451191	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 113,234,268-113,743,303 , GRCh38.p12 chr1: 112,691,646-113,200,681	MOV10, LRIG2, 19 more genes

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