arf1[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
nsv3899821	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr7: 94,399,796-94,606,785 , GRCh38.p12 chr7: 94,770,484-94,977,473	ARF1P1, GRPEL2P3, 2 more genes
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	RNU6-438P, LOC105375300, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	LOC107986817, DNAJB9, 2014 more genes
nsv3914094	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 84,002,634-95,228,883 , GRCh37 chr7: 83,631,950-94,858,195 , NCBI36 chr7: 83,469,886-94,696,131	LINC03017, MIR1285-1, 121 more genes
nsv4674115	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 223,653,722-234,591,807 , GRCh38.p12 chr1: 223,480,380-234,456,061	ARF1, LOC105373163, 258 more genes
nsv3892887	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 92,445,452-99,686,985 , GRCh38.p12 chr7: 92,816,138-100,089,362	LOC105375402, LOC112267858, 153 more genes
nsv3899452	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 224,439,448-231,074,857 , GRCh37 chr1: 226,372,825-233,008,234 , GRCh38 chr1: 226,185,124-232,872,488	ARF1, RNA5S10, 178 more genes
nsv6636271	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 92,721,627-98,311,537 , GRCh38.p12 chr7: 93,092,314-98,682,225	MARK2P10, PON2, 97 more genes
nsv3908695	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 221,587,658-226,810,656 , GRCh38 chr1: 223,347,693-228,556,332 , GRCh37 chr1: 223,521,035-228,744,033	ARF1, SNAP47, 137 more genes
nsv3899116	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 223,636,497-228,621,170 , GRCh38 chr1: 225,382,172-230,418,801 , GRCh37 chr1: 225,569,874-230,554,547	ARF1, ISCA1P2, 146 more genes
nsv3911538	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 92,226,394-97,035,894 , GRCh38 chr7: 92,759,144-97,568,646 , GRCh37 chr7: 92,388,458-97,197,958	LOC105375410, LOC107984034, 75 more genes
nsv6313841	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 228,214,912-231,483,538 , GRCh38.p12 chr1: 228,027,211-231,347,792	ARF1, ISCA1P2, 105 more genes
nsv3901032	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 93,700,162-96,950,914 , GRCh38.p12 chr7: 94,070,850-97,321,602	LOC105375404, LOC107984034, 52 more genes
nsv3908984	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 93,285,237-96,280,817 , GRCh38.p12 chr7: 93,655,925-96,651,505	LOC105375402, PPP1R9A-AS1, 51 more genes
nsv4685981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 93,516,132-95,668,733 , GRCh38.p12 chr7: 93,886,820-96,039,421	LOC105375404, BET1, 36 more genes
nsv3916221	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 92,754,488-94,797,369 , GRCh37.p13 chr7: 92,916,552-94,959,433 , GRCh38.p12 chr7: 93,287,240-95,330,121	BET1-AS1, RN7SKP129, 33 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	ARF1, MARK1, 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	ARF1, SNAP47, 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	ARF1, RNU1-153P, 4887 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	RNU6-565P, LAMB1, 2684 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 68

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Number of Variants: 20

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