trmt10a[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
nsv7096483	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 100,470,245-100,544,005 , GRCh38.p12 chr4: 99,549,088-99,622,848	TRMT10A, MTTP
nsv7097218	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 100,485,243-100,504,684 , GRCh38.p12 chr4: 99,564,086-99,583,527	TRMT10A, MTTP
nsv6311813	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 100,470,245-100,521,910 , GRCh38.p12 chr4: 99,549,088-99,600,753	TRMT10A, MTTP
nsv7096482	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 100,239,320-100,528,137 , GRCh38.p12 chr4: 99,318,163-99,606,980	TRMT10A, ADH1B, 5 more genes
nsv3923759	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 58,862,002-102,129,682 , GRCh37.p13 chr4: 59,167,245-101,910,659 , GRCh38.p12 chr4: 58,301,079-100,989,502	TRMT10A, EREG, 530 more genes
nsv3923733	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 80,427,023-100,855,441 , GRCh37 chr4: 81,348,177-101,776,598 , NCBI36 chr4: 81,567,201-101,995,621	TRMT10A, PDLIM5, 215 more genes
nsv3885328	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 92,201,567-103,043,808 , GRCh38.p12 chr4: 91,280,416-102,122,651	TRMT10A, TBCAP3, 86 more genes
nsv3910689	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 92,610,413-101,521,991 , GRCh37 chr4: 93,531,564-102,443,148 , NCBI36 chr4: 93,750,587-102,662,171	TRMT10A, GRID2, 77 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	TRMT10A, 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	TRMT10A, 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	TRMT10A, 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	TRMT10A, 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	TRMT10A, 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	TRMT10A, KLKB1, 1118 more genes
nsv6291432	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354	TRMT10A, SNHG27, 1091 more genes
nsv3920388	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 97,014,044-137,331,362 , NCBI36 chr4: 97,233,067-137,550,812 , GRCh38 chr4: 96,092,893-136,410,207	TRMT10A, MIR576, 447 more genes
nsv4729197	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 94,692,345-101,308,220 , GRCh38.p12 chr4: 93,771,194-100,387,063	TRMT10A, ADH1A, 66 more genes
nsv6291428	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 95,490,755-109,977,216 , GRCh38.p12 chr4: 94,569,604-109,056,060	TRMT10A, ADH1A, 157 more genes
nsv6311812	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 100,239,320-100,544,005 , GRCh38.p12 chr4: 99,318,163-99,622,848	TRMT10A, C4orf17, 5 more genes
nsv4456424	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 100,239,111-100,509,321 , GRCh38.p12 chr4: 99,317,954-99,588,164	TRMT10A, ADH7, 5 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 22

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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