snta1[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
nsv7096074	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 31,996,313-32,026,852 , GRCh38.p12 chr20: 33,408,507-33,439,046	SNTA1
nsv5381306	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 32,026,637-32,031,436 , GRCh38.p12 chr20: 33,438,831-33,443,630	SNTA1
nsv3912723	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 30,288,202-45,731,170 , GRCh37.p13 chr20: 30,824,541-46,297,763 , GRCh38.p12 chr20: 32,236,738-47,669,019	SNTA1, LOC107985448, 370 more genes
nsv3913594	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 32,020,169-35,450,284 , NCBI36 chr20: 31,483,830-34,883,698 , GRCh38 chr20: 33,432,363-36,821,881	SNTA1, AHCY, 93 more genes
nsv6311078	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 31,189,994-34,287,210 , GRCh38.p12 chr20: 32,602,192-35,699,288	SNTA1, EDEM2, 93 more genes
nsv3892750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941	SNTA1, 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	SNTA1, 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	SNTA1, 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	SNTA1, 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	SNTA1, 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	SNTA1, DYNLRB1, 555 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	SNTA1, 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	SNTA1, 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	SNTA1, EFCAB8, 162 more genes
nsv3920503	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr20: 32,062,768-35,906,606 , NCBI36 chr20: 30,114,232-33,957,942 , GRCh37 chr20: 30,650,571-34,494,528	SNTA1, UQCC1, 111 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	SNTA1, HAUS6P2, 78 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	SNTA1, AHCY, 330 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	SNTA1, 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	SNTA1, AHCY, 160 more genes
nsv3887865	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr20: 31,996,293-33,761,838 , GRCh38.p12 chr20: 33,408,487-35,174,035	SNTA1, EDEM2, 42 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 23

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Number of Variants: 20

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Supplemental Content

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Search details

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