mllt3[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
nsv3920346	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 20,370,585-20,468,576 , GRCh37 chr9: 20,380,585-20,478,576 , GRCh38 chr9: 20,380,587-20,478,578	MLLT3, MIR4473, 1 more genes
nsv3898933	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 20,439,837-20,538,919 , GRCh38.p12 chr9: 20,439,839-20,538,920	MLLT3, MIR4474, 1 more genes
nsv6313760	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 20,194,313-20,364,684 , GRCh38.p12 chr9: 20,194,315-20,364,686	MLLT3, SLC24A2, 1 more genes
nsv4455615	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 20,323,068-20,457,595 , GRCh38.p12 chr9: 20,323,070-20,457,597	MLLT3, SMNP, 2 more genes
nsv3905120	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 20,610,950-20,740,733 , GRCh38.p12 chr9: 20,610,951-20,740,734	MLLT3, FOCAD, 2 more genes
nsv3907179	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 20,407,662-20,489,380 , GRCh38.p12 chr9: 20,407,664-20,489,382	MLLT3, RNU4-26P, 1 more genes
nsv3914932	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 19,554,273-28,096,620 , GRCh37 chr9: 19,564,273-28,106,620 , GRCh38 chr9: 19,564,275-28,106,622	MLLT3, LINC01241, 103 more genes
nsv3912247	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981	MLLT3, ALOX15P2, 2184 more genes
nsv3890420	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,122,247 , GRCh38.p12 chr9: 10,590-138,231,797	MLLT3, TBC1D13, 2183 more genes
nsv3905118	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,114,095 , GRCh38.p12 chr9: 10,590-138,223,645	MLLT3, MIR219A2, 2183 more genes
nsv3891842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,107,672 , GRCh38.p12 chr9: 10,590-138,217,222	MLLT3, OR13C1P, 2183 more genes
nsv3895453	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 46,587-141,066,491 , GRCh38.p12 chr9: 46,587-138,172,039	MLLT3, RPL19P15, 2176 more genes
nsv3900967	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 163,131-141,122,114 , GRCh38.p12 chr9: 163,131-138,231,664	MLLT3, BANCR, 2173 more genes
nsv3907479	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 62,525-141,006,407 , GRCh38.p12 chr9: 62,525-138,111,955	MLLT3, OR2AM1P, 2174 more genes
nsv3922684	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897	MLLT3, TDRD7, 2170 more genes
nsv3919257	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 204,193-141,073,897 , GRCh38 chr9: 204,193-138,179,445 , NCBI36 chr9: 194,193-140,193,718	MLLT3, LOC107987031, 2169 more genes
nsv3915973	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr9: 193,412-138,159,073 , GRCh37 chr9: 68,420,641-141,053,525 , NCBI36 chr9: 67,910,461-140,173,346	MLLT3, CTNNAL1, 2170 more genes
nsv3911025	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 193,412-138,124,524 , NCBI36 chr9: 194,090-140,138,797 , GRCh37 chr9: 204,090-141,018,976	MLLT3, RORB-AS1, 2168 more genes
nsv3921598	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389	MLLT3, PGAP4, 2167 more genes
nsv4457273	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936	MLLT3, CDRT15P14, 2167 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 88

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Number of Variants: 20

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