rars1[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
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	RARS1, MEGF10, 2080 more genes
nsv3886151	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 154,886,174-169,757,448 , GRCh38.p12 chr5: 155,506,614-170,330,444	RARS1, CCNG1, 148 more genes
nsv4674945	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 156,347,980-169,959,880 , GRCh38.p12 chr5: 156,920,969-170,532,876	RARS1, LINC02227, 146 more genes
nsv3879307	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 164,207,156-172,799,124 , GRCh38.p12 chr5: 164,780,150-173,372,121	RARS1, RN7SL339P, 113 more genes
nsv4578263	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 166,420,934-173,324,844 , GRCh38.p12 chr5: 166,993,929-173,897,841	RARS1, LINC01187, 112 more genes
nsv7097266	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 167,849,013-169,661,202 , GRCh38.p12 chr5: 168,422,008-170,234,198	RARS1, FBLL1, 25 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	RARS1, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	RARS1, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	RARS1, SPEF2, 2490 more genes
nsv3874238	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 106,716,357-180,687,338 , GRCh38.p12 chr5: 107,380,656-181,260,337	RARS1, PJA2, 1228 more genes
nsv6315448	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788	RARS1, GRM6, 554 more genes
nsv3921182	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 149,094,155-180,699,152 , GRCh38 chr5: 149,714,592-181,272,151 , NCBI36 chr5: 149,074,348-180,631,758	RARS1, RN7SKP148, 553 more genes
nsv3885523	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 155,344,802-180,693,344 , GRCh38.p12 chr5: 155,917,792-181,266,343	RARS1, WWC1, 446 more genes
nsv3924400	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 156,185,101-180,629,412 , GRCh37 chr5: 156,252,523-180,696,806 , GRCh38 chr5: 156,825,512-181,269,805	RARS1, CEP192P1, 443 more genes
nsv6636891	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790	RARS1, EFCAB9, 287 more genes
nsv3921186	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 164,386,701-181,269,805 , GRCh37 chr5: 163,813,707-180,696,806 , NCBI36 chr5: 163,746,285-180,629,412	RARS1, TENM2, 347 more genes
nsv3920339	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 164,323,950-180,629,412 , GRCh37.p13 chr5: 164,391,372-180,696,806 , GRCh38.p12 chr5: 164,964,366-181,269,805	RARS1, MIR1229, 343 more genes
nsv4455586	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 156,597,181-171,166,353 , GRCh38.p12 chr5: 157,170,170-171,739,349	RARS1, LOC105377677, 164 more genes
nsv4729368	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr5: 166,378,793-170,174,830 , GRCh38.p12 chr5: 166,951,788-170,747,826	RARS1, DOCK2, 38 more genes
nsv3884275	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr5: 94,844,077-178,830,410 , GRCh38.p12 chr5: 95,508,373-179,403,409	RARS1, LOC107986368, 1258 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

Find related data

Search details

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