trib1[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
nsv3902676	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 126,082,565-126,611,303 , GRCh38.p12 chr8: 125,070,323-125,599,059	TRIB1, LINC02964, 3 more genes
nsv3903593	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 126,358,525-126,559,524 , GRCh38.p12 chr8: 125,346,283-125,547,282	TRIB1, NSMCE2, 1 more genes
nsv6637224	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 112,234,557-133,668,379 , GRCh38.p12 chr8: 111,222,328-132,656,133	TRIB1, RNU4-37P, 220 more genes
nsv3876297	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 114,508,086-129,040,004 , GRCh38.p12 chr8: 113,495,857-128,027,758	TRIB1, ZHX1-C8orf76, 172 more genes
nsv3914003	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 114,369,859-127,797,514 , GRCh38 chr8: 113,288,454-126,716,087 , GRCh37 chr8: 114,300,683-127,728,332	TRIB1, RNU6-442P, 154 more genes
nsv4455511	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 124,120,772-135,265,846 , GRCh38.p12 chr8: 123,108,532-134,253,603	TRIB1, MTSS1, 148 more genes
nsv7148124	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 118,185,471-126,635,744 , GRCh38.p12 chr8: 117,173,232-125,623,500	TRIB1, LINC02964, 115 more genes
nsv4457220	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 123,074,293-131,113,892 , GRCh38.p12 chr8: 122,062,054-130,101,646	TRIB1, ZHX1-C8orf76, 117 more genes
nsv3915173	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636	TRIB1, RN7SL474P, 2109 more genes
nsv3901821	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028	TRIB1, TBC1D31, 2109 more genes
nsv4349554	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385	TRIB1, LOC101929488, 2105 more genes
nsv3916777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575	TRIB1, RPL5P22, 2105 more genes
nsv3898123	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385	TRIB1, SPAG1, 2105 more genes
nsv3908608	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 164,984-146,293,414 , GRCh38.p12 chr8: 214,984-145,068,028	TRIB1, LINC01617, 2105 more genes
nsv3893757	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 158,991-146,280,828 , GRCh38.p12 chr8: 208,991-145,055,442	TRIB1, LOC105375890, 2105 more genes
nsv3923310	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098	TRIB1, LOC112268023, 2105 more genes
nsv3914307	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 191,605-146,280,167 , GRCh38 chr8: 241,605-145,054,781 , NCBI36 chr8: 181,605-146,250,971	TRIB1, LOC107986897, 2104 more genes
nsv3919282	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824	TRIB1, MIR4662B, 2104 more genes
nsv3919200	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639	TRIB1, LOC112268023, 2103 more genes
nsv3906425	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 12,490,999-146,295,771 , GRCh38.p12 chr8: 12,633,490-145,070,385	TRIB1, LOC112268016, 1819 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 53

Page of 3

Number of Variants: 20

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Supplemental Content

Find related data

Search details

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