asrgl1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 18

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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
nsv6309439	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 62,105,450-62,124,636 , GRCh38.p12 chr11: 62,337,978-62,357,164	ASRGL1
nsv7094091	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 62,156,585-62,159,756 , GRCh38.p12 chr11: 62,389,113-62,392,284	ASRGL1
nsv5380888	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 62,105,450-62,156,743 , GRCh38.p12 chr11: 62,337,978-62,389,271	ASRGL1, RCC2P6
nsv3902179	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 62,096,355-62,139,467 , GRCh38.p12 chr11: 62,328,883-62,371,995	ASRGL1, NPM1P35, 1 more genes
nsv3903102	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 62,099,144-62,139,467 , GRCh38.p12 chr11: 62,331,672-62,371,995	ASRGL1, RCC2P6, 1 more genes
nsv4729063	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 62,010,938-62,116,409 , GRCh38.p12 chr11: 62,243,466-62,348,937	ASRGL1, SCGB1D2, 3 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	ASRGL1, FAUP4, 2031 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	ASRGL1, LOC105376598, 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	ASRGL1, RTN3, 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	ASRGL1, IGHMBP2, 2829 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	ASRGL1, PYGM, 2125 more genes
nsv3912559	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 62,249,520-62,946,093 , GRCh37 chr11: 62,016,992-62,713,565 , NCBI36 chr11: 61,773,568-62,470,141	ASRGL1, SNORD28, 53 more genes
nsv3909634	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 61,840,997-62,987,330 , GRCh38.p12 chr11: 62,073,525-63,219,858	ASRGL1, CHRM1, 66 more genes
nsv3890886	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 58,935,215-62,177,656 , GRCh38.p12 chr11: 59,167,742-62,410,184	ASRGL1, MYRF, 137 more genes
nsv3901327	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 62,157,418-62,362,465 , GRCh38.p12 chr11: 62,389,946-62,594,993	ASRGL1, MTA2, 6 more genes
nsv7093694	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878	ASRGL1, VPS37C, 298 more genes
nsv4675148	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 60,385,382-62,456,278 , GRCh38.p12 chr11: 60,617,909-62,688,806	ASRGL1, LOC105369326, 91 more genes
nsv4729555	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 61,874,941-62,236,378 , GRCh38.p12 chr11: 62,107,469-62,468,906	ASRGL1, INCENP, 11 more genes

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