arg1[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
nsv4450916	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 131,576,653-131,583,918 , GRCh37 chr6: 131,897,793-131,905,058	ARG1, MED23
nsv7097418	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 131,900,217-131,902,528 , GRCh38.p12 chr6: 131,579,077-131,581,388	ARG1, MED23
nsv6312310	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 131,903,580-131,903,817 , GRCh38 chr6: 131,582,440-131,582,677	ARG1, MED23
nsv3924851	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr6: 131,840,288-131,958,837 , GRCh37 chr6: 131,798,595-131,917,144 , GRCh38 chr6: 131,477,455-131,596,004	ARG1, MED23
nsv4456021	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 131,905,716-131,915,353 , GRCh38.p12 chr6: 131,584,576-131,594,213	ARG1, MED23
nsv6312232	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 131,894,423-131,903,875 , GRCh38.p12 chr6: 131,573,283-131,582,735	ARG1, MED23
nsv7097809	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 131,902,339-131,905,048 , GRCh38.p12 chr6: 131,581,199-131,583,908	ARG1, MED23
nsv7093523	insertion	1	nstd102	human	Uncertain significance	GRCh38 chr6: 131,576,727-131,576,727 , GRCh37 chr6: 131,897,867-131,897,867	ARG1, MED23
nsv3920683	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 109,372,795-132,430,553 , GRCh37 chr6: 109,266,102-132,388,860 , GRCh38 chr6: 108,944,899-132,067,720	ARG1, SSXP10, 298 more genes
nsv6315321	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 115,941,808-133,892,653 , GRCh37.p13 chr6: 116,262,971-134,213,791	ARG1, SLC18B1, 223 more genes
nsv3871408	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 131,388,023-137,469,640 , GRCh38.p12 chr6: 131,066,883-137,148,503	ARG1, LOC105378012, 108 more genes
nsv6290946	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 130,769,034-136,009,217 , GRCh38.p12 chr6: 130,447,889-135,688,079	ARG1, LOC105378004, 89 more genes
nsv3891425	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 28,623,965-33,361,042 , GRCh37 chr1: 28,751,378-33,588,455 , GRCh38 chr1: 28,424,867-33,122,854	SNHG3, LOC105378620, 115 more genes
nsv3895257	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 31,239,605-33,825,029 , NCBI36 chr1: 31,012,192-33,597,616 , GRCh38 chr1: 30,766,758-33,359,428	LOC105378623, TINAGL1, 85 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	MARK1, LINC02766, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	SNAP47, STK40, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	RNU1-153P, MIR3917, 4887 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	ARG1, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	ARG1, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	ARG1, SOD1P1, 2905 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 42

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Number of Variants: 20

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