gata2[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
nsv3887897	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 128,479,422-128,487,076 , GRCh37 chr3: 128,198,265-128,205,919	GATA2
nsv6112699	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 128,201,205-128,203,154 , GRCh38.p12 chr3: 128,482,362-128,484,311	GATA2
nsv6112683	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 128,199,862-128,200,787 , GRCh38.p12 chr3: 128,481,019-128,481,944	GATA2
nsv6112684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 128,200,107-128,200,462 , GRCh38 chr3: 128,481,264-128,481,619	GATA2
nsv4454541	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 128,486,793-128,487,041 , GRCh37 chr3: 128,205,636-128,205,884	GATA2
nsv7093255	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 128,481,765-128,481,836 , GRCh37 chr3: 128,200,608-128,200,679	GATA2
nsv3883777	copy number variation	2	nstd102	human	Pathogenic, Likely pathogenic	GRCh38 chr3: 128,483,320-128,483,347 , GRCh37 chr3: 128,202,163-128,202,190	GATA2
nsv5381359	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr3: 128,199,862-128,205,874 , GRCh38.p12 chr3: 128,481,019-128,487,031	GATA2
nsv5564188	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 128,198,104-128,205,874 , GRCh38.p12 chr3: 128,479,261-128,487,031	GATA2
nsv5381412	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 128,198,104-128,205,221 , GRCh38.p12 chr3: 128,479,261-128,486,378	GATA2
nsv4681803	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 128,199,852-128,205,884 , GRCh38.p12 chr3: 128,481,009-128,487,041	GATA2
nsv3873425	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr3: 128,483,850-128,487,041 , GRCh37 chr3: 128,202,693-128,205,884	GATA2
nsv7093128	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 128,200,717-128,200,718 , GRCh38 chr3: 128,481,874-128,481,875	GATA2
nsv3873876	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 128,204,043-128,206,074 , GRCh38 chr3: 128,485,200-128,487,231	GATA2, GATA2-AS1
nsv1397907	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chr3: 128,198,265-128,212,030 , GRCh38.p12 chr3: 128,479,422-128,493,187	GATA2, GATA2-AS1
nsv6112664	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 128,170,000-128,230,000 , GRCh38.p12 chr3: 128,451,157-128,511,157	GATA2, GATA2-AS1, 3 more genes
nsv6112693	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 128,181,289-128,205,514 , GRCh38.p12 chr3: 128,462,446-128,486,671	GATA2, DNAJB8, 1 more genes
nsv3918094	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 113,822,514-129,935,667 , GRCh38 chr3: 112,620,977-128,734,134 , GRCh37 chr3: 112,339,824-128,452,977	GATA2, QTRT2, 284 more genes
nsv6311770	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 120,365,818-133,465,047 , GRCh38.p12 chr3: 120,646,971-133,746,203	GATA2, HNRNPA1P23, 278 more genes
nsv6112714	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481	GATA2, RNU6-789P, 169 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 36

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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