ubxn8[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
nsv3893393	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 30,604,385-30,612,779 , GRCh38.p12 chr8: 30,746,868-30,755,262	UBXN8
nsv3899253	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 30,604,495-30,609,061 , GRCh38.p12 chr8: 30,746,978-30,751,544	UBXN8
nsv3897942	copy number variation	1	nstd102	human	Benign	GRCh37 chr8: 30,601,758-30,605,320 , GRCh38.p12 chr8: 30,744,241-30,747,803	UBXN8, LOC105379356
nsv6636795	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr8: 30,564,838-30,618,334 , GRCh38.p12 chr8: 30,707,321-30,760,817	UBXN8, LOC105379355, 2 more genes
nsv3916527	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr8: 15,137,722-32,366,274 , GRCh37.p13 chr8: 15,093,351-32,246,732 , GRCh38.p12 chr8: 15,235,842-32,389,216	UBXN8, LOC105379343, 281 more genes
nsv3923174	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 18,972,996-33,619,264 , GRCh37 chr8: 18,830,506-33,476,782 , NCBI36 chr8: 18,874,786-33,596,324	UBXN8, RPLP1P9, 259 more genes
nsv6637025	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 26,808,969-38,346,383 , GRCh38.p12 chr8: 26,951,452-38,488,865	UBXN8, LINC02948, 185 more genes
nsv3918177	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 29,362,097-40,231,708 , NCBI36 chr8: 29,275,533-40,208,384 , GRCh37 chr8: 29,219,614-40,089,227	UBXN8, RPL23P10, 159 more genes
nsv3919731	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 25,171,103-31,750,600 , NCBI36 chr8: 25,084,535-31,727,658 , GRCh37 chr8: 25,028,618-31,608,116	UBXN8, LOC100131127, 122 more genes
nsv3923302	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 24,910,364-31,210,737 , NCBI36 chr8: 24,823,781-31,187,795 , GRCh37 chr8: 24,767,877-31,068,253	UBXN8, BNIP3L, 123 more genes
nsv3911687	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr8: 24,910,364-31,196,357 , NCBI36 chr8: 24,823,781-31,173,415 , GRCh37 chr8: 24,767,877-31,053,873	UBXN8, EXTL3-AS1, 123 more genes
nsv3899293	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr8: 30,335,124-33,770,070 , GRCh38.p12 chr8: 30,477,608-33,912,552	UBXN8, NRG1, 46 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	UBXN8, 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	UBXN8, 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	UBXN8, 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	UBXN8, 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	UBXN8, 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	UBXN8, 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	UBXN8, 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	UBXN8, LOC112268023, 2105 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 69

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Number of Variants: 20

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