mnd1[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
nsv4674402	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 154,316,483-154,325,120 , GRCh38.p12 chr4: 153,395,331-153,403,968	MND1
nsv3874224	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 153,203,431-162,912,359 , GRCh38.p12 chr4: 152,282,279-161,991,207	MND1, PLRG1, 120 more genes
nsv3873978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724	MND1, LOC100422029, 2358 more genes
nsv3876533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611	MND1, LOC100420289, 2347 more genes
nsv3884499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286	MND1, MTND4LP29, 2341 more genes
nsv3880085	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318	MND1, LOC112268460, 2345 more genes
nsv3883791	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495	MND1, LOC105377343, 2341 more genes
nsv3875534	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 93,071,152-190,957,473 , GRCh38.p12 chr4: 92,150,001-190,036,318	MND1, KLKB1, 1118 more genes
nsv3874596	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 109,199,664-189,752,726 , GRCh38.p12 chr4: 108,278,508-188,831,572	MND1, RPL6P12, 938 more genes
nsv3924008	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 118,065,569-190,042,639 , GRCh37 chr4: 118,986,724-190,828,225 , NCBI36 chr4: 119,206,172-191,200,788	MND1, PPID, 828 more genes
nsv3874610	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 119,437,495-190,904,301 , GRCh38.p12 chr4: 118,516,340-189,983,146	MND1, OTUD4, 813 more genes
nsv3918110	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 122,658,828-191,220,419 , GRCh38 chr4: 121,518,223-190,062,270 , GRCh37 chr4: 122,439,378-190,828,225	MND1, SCRG1, 770 more genes
nsv4455301	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 124,873,497-185,278,662 , GRCh38.p12 chr4: 123,952,342-184,357,509	MND1, SMARCA5, 633 more genes
nsv3911855	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 125,432,943-185,761,887 , GRCh37 chr4: 126,354,098-186,683,041 , NCBI36 chr4: 126,573,548-186,920,035	MND1, RPL26P16, 656 more genes
nsv3911177	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 131,985,253-190,095,391 , NCBI36 chr4: 133,125,858-191,250,527 , GRCh37 chr4: 132,906,408-190,828,225	MND1, SNORD73B, 683 more genes
nsv3914528	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 136,076,221-191,194,467 , GRCh38 chr4: 134,935,616-190,036,318 , GRCh37 chr4: 135,856,771-190,957,473	MND1, ATP5MGP4, 660 more genes
nsv3922745	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 139,651,136-191,121,344 , GRCh37 chr4: 139,431,686-190,828,225 , GRCh38 chr4: 138,510,532-189,963,195	MND1, TMEM131L, 622 more genes
nsv3871834	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 136,912,336-184,253,252 , GRCh38.p12 chr4: 135,991,181-183,332,099	MND1, LOC105377452, 526 more genes
nsv3916456	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 145,042,668-189,975,519 , NCBI36 chr4: 146,183,270-191,133,668 , GRCh37 chr4: 145,963,820-190,828,225	MND1, LOC107986328, 546 more genes
nsv3882398	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 147,287,237-191,133,858 , GRCh37.p13 chr4: 147,067,787-190,896,864 , GRCh38.p12 chr4: 146,146,635-189,975,709	MND1, LOC105377519, 526 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 31

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Number of Variants: 20

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Supplemental Content

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Search details

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