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

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3902316	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 13,299,425-13,299,657 , GRCh38.p12 chr11: 13,277,878-13,278,110	BMAL1
nsv3908420	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 13,299,016-13,310,801 , GRCh38.p12 chr11: 13,277,469-13,289,254	BMAL1
nsv3906731	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 13,299,016-13,299,657 , GRCh38.p12 chr11: 13,277,469-13,278,110	BMAL1
nsv3908840	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 13,299,016-13,299,325 , GRCh38.p12 chr11: 13,277,469-13,277,778	BMAL1
nsv3891857	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 13,337,750-13,457,670 , GRCh38.p12 chr11: 13,316,203-13,436,123	BMAL1, RN7SKP151, 1 more genes
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	FAUP4, MMP7, 2031 more genes
nsv3915585	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 9,967,639-16,803,929 , GRCh37 chr11: 10,011,063-16,847,353 , GRCh38 chr11: 9,989,516-16,825,806	BTBD10, LOC107984370, 86 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	LOC105376598, OSBPL9P2, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	RTN3, KRTAP5-13P, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	IGHMBP2, SYTL2, 2829 more genes
nsv3898926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-37,698,540 , GRCh38.p12 chr11: 230,615-37,676,990	OR51L1, OR52V1P, 771 more genes
nsv4674879	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449	BGLT3, RPL21P97, 723 more genes
nsv3906221	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673	PCNAP4, LIN7C, 688 more genes
nsv6315535	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599	OR52Q1P, RNU6-593P, 630 more genes
nsv3894525	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-25,584,362 , GRCh38.p12 chr11: 230,615-25,562,816	SDHCP4, SWAP70, 620 more genes
nsv4674824	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344	SNORA88, LINC02729, 305 more genes
nsv3912558	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 446,754-18,926,289 , GRCh38 chr11: 446,754-18,904,742 , NCBI36 chr11: 436,754-18,882,865	TRIM22, CSNK2A3, 546 more genes
nsv3898948	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 230,615-17,099,213 , GRCh38.p12 chr11: 230,615-17,077,666	MTND5P21, IFITM1, 506 more genes
nsv3912175	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 10,107,142-14,047,625 , GRCh37.p13 chr11: 10,150,566-14,091,049 , GRCh38.p12 chr11: 10,129,019-14,069,502	LINC02545, CENPUP1, 58 more genes

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