asxl3[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5673057	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr18: 31,316,158-31,321,355 , GRCh38 chr18: 33,736,194-33,741,391	ASXL3
nsv4768305	copy number variation	2	nstd102	human	Likely pathogenic	GRCh37 chr18: 31,324,651-31,324,702 , GRCh38 chr18: 33,744,687-33,744,738	ASXL3
nsv6637953	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 31,107,959-31,289,885 , GRCh38.p12 chr18: 33,527,995-33,709,921	ASXL3
nsv6637823	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 30,988,810-31,359,711 , GRCh38.p12 chr18: 33,408,846-33,779,747	ASXL3, CCDC178
nsv3170355	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chr18: 31,158,541-31,331,158 , GRCh38.p12 chr18: 33,578,577-33,751,194	ASXL3, LOC107985157
nsv4457778	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 30,863,773-31,433,693 , GRCh38.p12 chr18: 33,283,809-33,853,729	ASXL3, NOL4, 1 more genes
nsv4768359	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 30,863,773-31,433,693 , GRCh38.p12 chr3: 30,822,281-31,392,201	GADL1, CNN2P6, 4 more genes
nsv6314722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520	ASXL3, LOC107985176, 632 more genes
nsv3900710	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 20,069,932-36,887,326 , GRCh38.p12 chr18: 22,489,969-39,307,362	ASXL3, CABLES1, 174 more genes
nsv3912224	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 27,945,491-39,904,182 , GRCh38 chr18: 32,111,530-44,070,219 , GRCh37 chr18: 29,691,493-41,650,184	ASXL3, SYT4, 94 more genes
nsv4676233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 22,868,759-34,335,753 , GRCh38.p12 chr18: 25,288,795-36,755,790	ASXL3, DHFRP1, 116 more genes
nsv3912888	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 27,024,475-37,983,616 , NCBI36 chr18: 25,278,473-36,237,614 , GRCh38 chr18: 29,444,510-40,403,652	ASXL3, KLHL14, 107 more genes
nsv4729854	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 23,971,647-33,737,300 , GRCh38.p12 chr18: 26,391,683-36,157,337	ASXL3, CLUHP6, 100 more genes
nsv3897721	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 29,711,972-35,866,193 , GRCh38.p12 chr18: 32,132,009-38,286,229	ASXL3, LOC105372073, 56 more genes
nsv6315530	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271	ASXL3, LOC105372145, 947 more genes
nsv3907444	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 12,842-78,015,180 , GRCh38.p12 chr18: 12,842-80,257,297	ASXL3, GALNT1, 947 more genes
nsv3890669	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 13,034-78,015,180 , GRCh38.p12 chr18: 13,034-80,257,297	ASXL3, MYL12B, 947 more genes
nsv3918488	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 43,345-76,068,860 , GRCh38 chr18: 53,345-80,209,986 , GRCh37 chr18: 53,345-77,967,869	ASXL3, LOC105372027, 945 more genes
nsv3924351	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 108,760-76,113,817 , GRCh38 chr18: 118,760-80,254,946 , GRCh37 chr18: 118,760-78,012,829	ASXL3, MIX23P1, 942 more genes
nsv3919004	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 136,226-80,256,240 , GRCh37 chr18: 136,226-78,014,123 , NCBI36 chr18: 126,226-76,115,097	ASXL3, LIVAR, 941 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 48

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Number of Variants: 20

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