rpl37a[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
nsv7096239	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 217,279,428-217,347,700 , GRCh38.p12 chr2: 216,414,705-216,482,977	RPL37A-DT, SMARCAL1
nsv3922354	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 52,476,150-52,542,042 , GRCh37.p13 chr4: 52,781,393-52,847,285 , GRCh38.p12 chr4: 51,915,227-51,981,119	RPL37AP2, DCUN1D4
nsv6312421	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 107,002,458-107,204,434 , GRCh38.p12 chr7: 107,362,013-107,563,989 , GRCh38.p12 chr7\|NW_017852930.1: 207,539-409,644	COG5, DUS4L-BCAP29, 3 more genes
nsv7097469	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 106,921,725-107,167,822 , GRCh38.p12 chr7: 107,281,280-107,527,377 , GRCh38.p12 chr7\|NW_017852930.1: 126,802-373,032	GPR22, RPL37AP6, 1 more genes
nsv4457258	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 107,014,544-107,115,209 , GRCh38.p12 chr7\|NW_017852930.1: 219,629-320,412 , GRCh38.p12 chr7: 107,374,099-107,474,764	COG5, RPL37AP6, 1 more genes
nsv4457326	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 12,929,249-13,022,464 , GRCh38.p12 chr12: 12,776,315-12,869,530	RPL37AP9, APOLD1, 2 more genes
nsv7096260	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 43,047,045-43,280,248 , GRCh38.p12 chr20: 44,418,405-44,651,607	ADA, HNF4A, 6 more genes
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	RPL37A, DAZAP2P1, 2991 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
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	FAUP4, MMP7, 2031 more genes
nsv3880626	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 85,988,428-120,548,687 , GRCh38.p12 chr6: 85,278,710-120,227,541	LOC107986534, FYN, 426 more genes
nsv3904761	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 80,053,454-113,316,236 , GRCh38.p12 chr11: 80,342,410-113,445,514	RPS6P16, CTSC, 449 more genes
nsv4675615	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620	ATG9B, OR10AC1, 603 more genes
nsv6313858	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488	RN7SL509P, LAMA4, 311 more genes
nsv3910101	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr11: 87,796,211-113,996,548 , GRCh37.p13 chr11: 88,156,563-114,491,338 , GRCh38.p12 chr11: 88,423,395-114,620,616	PHB1P16, LOC100418884, 385 more genes
nsv3924576	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 97,164,591-122,524,393 , GRCh38 chr6: 96,609,994-122,161,548 , GRCh37 chr6: 97,057,870-122,482,694	TUBE1, PLN, 318 more genes
nsv5674237	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872	FTLP10, RNU6-410P, 335 more genes
nsv3915633	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 134,002,121-158,077,335 , GRCh38 chr7: 134,666,829-158,591,882 , GRCh37 chr7: 134,351,581-158,384,574	MOXD2P, CALD1, 561 more genes
nsv3876958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 95,549,951-116,684,929 , GRCh38.p12 chr6: 94,840,233-116,363,766	LIN28B-AS1, SEC63, 258 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 273

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Number of Variants: 20

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