larp1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 19

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Number of Variants: 19

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	LARP1, MEGF10, 2080 more genes
nsv3912937	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 105,955,289-155,551,397 , NCBI36 chr5: 105,983,188-155,483,975 , GRCh38 chr5: 106,619,588-156,124,387	LARP1, LINC01023, 783 more genes
nsv3922783	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 152,761,187-167,248,053 , NCBI36 chr5: 152,120,940-166,607,636 , GRCh37 chr5: 152,140,747-166,675,058	LARP1, APOOP1, 151 more genes
nsv3915958	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 152,443,869-166,104,392 , NCBI36 chr5: 151,803,623-165,463,975 , GRCh37 chr5: 151,823,430-165,531,397	LARP1, C5orf52, 147 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	LARP1, 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	LARP1, 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	LARP1, 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	LARP1, 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	LARP1, 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	LARP1, RN7SKP148, 553 more genes
nsv3878636	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 130,125,085-157,574,910 , GRCh38.p12 chr5: 130,789,392-158,147,902	LARP1, LOC100288484, 551 more genes
nsv3923414	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 130,196,621-154,701,371 , NCBI36 chr5: 130,224,520-154,681,564 , GRCh38 chr5: 130,860,928-155,321,811	LARP1, HNRNPA3P7, 514 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	LARP1, EFCAB9, 287 more genes
nsv3914878	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 146,520,648-163,194,778 , GRCh37.p13 chr5: 146,540,455-163,262,200 , GRCh38.p12 chr5: 147,160,892-163,835,194	LARP1, LOC105378231, 247 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	LARP1, LOC107986368, 1258 more genes
nsv4675503	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 154,117,774-154,339,494 , GRCh38.p12 chr5: 154,738,214-154,959,934	LARP1, GEMIN5, 5 more genes
nsv4455082	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 153,785,664-156,189,369 , GRCh38.p12 chr5: 154,406,104-156,762,358	LARP1, CNOT8, 25 more genes
nsv4729264	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 153,933,226-154,184,148 , GRCh38.p12 chr5: 154,553,666-154,804,588	LARP1, MIR3141, 5 more genes
nsv3912593	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259	LARP1, LOC105378993, 2492 more genes

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