tmtc1[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
nsv3901917	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 29,844,628-29,851,920 , GRCh38.p12 chr12: 29,691,695-29,698,987	TMTC1
nsv3907076	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 29,844,526-29,846,251 , GRCh38.p12 chr12: 29,691,593-29,693,318	TMTC1
nsv3898906	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr12: 29,829,853-30,013,033 , GRCh38.p12 chr12: 29,676,920-29,860,100	TMTC1
nsv3922122	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr12: 29,676,920-29,800,305 , GRCh37 chr12: 29,829,853-29,953,238 , NCBI36 chr12: 29,721,120-29,844,505	TMTC1
nsv3905973	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 29,773,141-29,840,353 , GRCh38.p12 chr12: 29,620,208-29,687,420	TMTC1, RPL21P99
nsv6314368	complex chromosomal rearrangement	6	nstd102	human	Pathogenic	GRCh37 chr12: 29,249,483-29,249,483 , GRCh37 chr12: 60,618,816-60,618,816 , GRCh37 chr12: 22,632,423-22,632,423 , GRCh37 chr12: 22,632,423-22,632,423 , GRCh37 chr12: 28,964,012-28,964,012 , GRCh37 chr12: 29,249,483-29,249,483 , GRCh37 chr12: 60,618,816-60,618,816 , GRCh37 chr12: 29,773,582-29,773,582 , GRCh37 chr12: 29,773,582-29,773,582 , GRCh37 chr12: 28,964,012-28,964,012 , GRCh37 chr12: 59,483,503-59,483,503 , GRCh37 chr12: 59,483,503-59,483,503 , GRCh38.p12 chr12: 22,479,489-22,479,489 , GRCh38.p12 chr12: 28,811,079-28,811,079 , GRCh38.p12 chr12: 29,620,649-29,620,649 , GRCh38.p12 chr12: 60,225,035-60,225,035 , GRCh38.p12 chr12: 60,225,035-60,225,035 , GRCh38.p12 chr12: 59,089,722-59,089,722 , GRCh38.p12 chr12: 28,811,079-28,811,079 , GRCh38.p12 chr12: 29,096,550-29,096,550 , GRCh38.p12 chr12: 29,096,550-29,096,550 , GRCh38.p12 chr12: 22,479,489-22,479,489 , GRCh38.p12 chr12: 29,620,649-29,620,649 , GRCh38.p12 chr12: 59,089,722-59,089,722	TMTC1, C2CD5, 1 more genes
nsv4729456	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 29,808,668-30,069,269 , GRCh38.p12 chr12: 29,655,735-29,916,336	TMTC1, LOC105369716, 2 more genes
nsv4675730	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 29,898,898-30,095,144 , GRCh38.p12 chr12: 29,745,965-29,942,211	TMTC1, LOC105369716, 1 more genes
nsv3911660	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr12: 29,583,681-30,137,476 , GRCh38 chr12: 29,539,481-30,093,276 , GRCh37 chr12: 29,692,414-30,246,209	TMTC1, LOC105369716, 2 more genes
nsv3912952	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 25,308,034-34,108,730 , GRCh38 chr12: 25,263,833-34,064,528 , GRCh37 chr12: 25,416,767-34,217,463	TMTC1, LOC101060058, 125 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	TMTC1, RNA5SP369, 2454 more genes
nsv3905447	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316	TMTC1, LOH12CR2, 2452 more genes
nsv3897722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059	TMTC1, RNU4ATAC16P, 2452 more genes
nsv3914194	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807	TMTC1, BTG1P1, 2451 more genes
nsv3904719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532	TMTC1, OR5BT1P, 2441 more genes
nsv3914427	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 18,636-36,150,744 , GRCh37.p13 chr12: 148,375-37,864,477 , GRCh38.p12 chr12: 43,334-37,470,675	TMTC1, LOC105369667, 684 more genes
nsv3905633	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-37,869,301 , GRCh38.p12 chr12: 64,620-37,475,499	TMTC1, RESF1, 684 more genes
nsv3897151	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-37,869,107 , GRCh38.p12 chr12: 64,620-37,475,305	TMTC1, CACNA2D4, 684 more genes
nsv4674941	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499	TMTC1, LOC105376675, 682 more genes
nsv3924262	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-34,835,837 , GRCh38 chr12: 64,620-34,682,902 , NCBI36 chr12: 44,047-34,727,104	TMTC1, ENO2, 684 more genes

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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 40

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Number of Variants: 20

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Supplemental Content

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