tpx2[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
nsv3892750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941	TPX2, TGIF2-RAB5IF, 1314 more genes
nsv3905072	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435	TPX2, LRRN4, 1313 more genes
nsv3895314	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202	TPX2, PKIG, 1311 more genes
nsv3896520	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110	TPX2, COMMD7, 1311 more genes
nsv3920218	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118	TPX2, MIR3646, 1310 more genes
nsv3910142	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 9,792,081-37,945,599 , GRCh38 chr20: 9,811,433-39,316,956 , NCBI36 chr20: 9,740,081-37,379,013	TPX2, DYNLRB1, 555 more genes
nsv3904899	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 17,705,775-31,600,738 , GRCh38.p12 chr20: 17,725,130-33,012,932	TPX2, TTLL9, 297 more genes
nsv3878906	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 17,705,775-31,600,738 , GRCh38.p12 chr20: 17,725,130-33,012,932	TPX2, KIF3B, 297 more genes
nsv3918053	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 25,703,100-38,491,480 , GRCh37.p13 chr20: 25,755,100-39,058,066 , GRCh38.p12 chr20: 25,774,464-40,429,426	TPX2, MYH7B, 300 more genes
nsv6313956	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 25,442,597-33,761,550 , GRCh38.p12 chr20: 25,461,961-35,173,747	TPX2, LOC105372586, 193 more genes
nsv4457806	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 29,833,608-35,087,952 , GRCh38.p12 chr20: 31,245,805-36,459,549	TPX2, EFCAB8, 162 more genes
nsv3917138	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 31,254,983-33,473,080 , NCBI36 chr20: 29,306,447-31,524,547 , GRCh37 chr20: 29,842,786-32,060,886	TPX2, HAUS6P2, 78 more genes
nsv3912259	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 31,254,983-32,575,288 , NCBI36 chr20: 29,306,447-30,626,751 , GRCh37 chr20: 29,842,786-31,163,090	TPX2, RNA5SP482, 51 more genes
nsv6291578	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 18,665,879-33,903,216 , GRCh38.p12 chr20: 18,685,235-35,315,413	TPX2, AHCY, 330 more genes
nsv4729757	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 19,750,804-30,479,077 , GRCh38.p12 chr20: 19,770,160-31,891,274	TPX2, BCL2L1, 222 more genes
nsv3897443	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 24,162,775-31,820,857 , GRCh38.p12 chr20: 24,182,139-33,233,051	TPX2, BCL2L1, 165 more genes
nsv6637546	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 29,652,122-35,603,726 , GRCh38.p12 chr20: 30,417,446-36,975,323	TPX2, AHCY, 195 more genes
nsv6637725	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 29,833,535-34,815,537 , GRCh38.p12 chr20: 31,245,732-36,227,615	TPX2, AHCY, 160 more genes
nsv3922338	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr20: 29,297,047-30,068,749 , GRCh37 chr20: 29,833,386-30,605,088 , GRCh38 chr20: 31,245,583-32,017,285	TPX2, BCL2L1, 38 more genes
nsv6291628	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr20: 30,239,509-30,494,851 , GRCh38.p12 chr20: 31,651,706-31,907,048	TPX2, BCL2L1, 7 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 27

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Number of Variants: 20

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Supplemental Content

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Search details

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