cog5[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
nsv7097598	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 106,843,961-107,053,097 , GRCh38.p12 chr7: 107,203,516-107,412,652 , GRCh38.p12 chr7\|NW_017852930.1: 49,038-258,175	COG5
nsv6312418	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 106,897,157-107,002,885 , GRCh38.p12 chr7: 107,256,712-107,362,440 , GRCh38.p12 chr7\|NW_017852930.1: 102,234-207,966	COG5
nsv4457042	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 106,868,531-106,927,676 , GRCh38.p12 chr7\|NW_017852930.1: 73,608-132,753 , GRCh38.p12 chr7: 107,228,086-107,287,231	COG5
nsv6312079	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 107,002,458-107,053,097 , GRCh38.p12 chr7\|NW_017852930.1: 207,539-258,175 , GRCh38.p12 chr7: 107,362,013-107,412,652	COG5
nsv6312078	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 106,897,157-106,938,811 , GRCh38.p12 chr7: 107,256,712-107,298,366 , GRCh38.p12 chr7\|NW_017852930.1: 102,234-143,888	COG5
nsv7097468	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 106,921,725-106,924,197 , GRCh38.p12 chr7: 107,281,280-107,283,752 , GRCh38.p12 chr7\|NW_017852930.1: 126,802-129,274	COG5
nsv6312420	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 107,002,458-107,002,885 , GRCh38.p12 chr7\|NW_017852930.1: 207,539-207,966 , GRCh38.p12 chr7: 107,362,013-107,362,440	COG5
nsv6312314	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 107,052,927-107,053,097 , GRCh38.p12 chr7\|NW_017852930.1: 258,007-258,175 , GRCh38.p12 chr7: 107,412,482-107,412,652	COG5
nsv6312315	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 107,167,662-107,167,822 , GRCh38.p12 chr7\|NW_017852930.1: 372,872-373,032 , GRCh38.p12 chr7: 107,527,217-107,527,377	COG5
nsv7097600	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 106,964,865-106,964,986 , GRCh38.p12 chr7: 107,324,420-107,324,541 , GRCh38.p12 chr7\|NW_017852930.1: 169,942-170,063	COG5
nsv6312517	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr7: 106,888,821-106,898,848 , GRCh38.p12 chr7: 107,248,376-107,258,403 , GRCh38.p12 chr7\|NW_017852930.1: 93,898-103,925	COG5
nsv7097599	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 106,876,875-107,013,225 , GRCh38.p12 chr7: 107,236,430-107,372,780 , GRCh38.p12 chr7\|NW_017852930.1: 81,952-218,310	COG5
nsv6312419	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 106,921,725-106,964,986 , GRCh38.p12 chr7\|NW_017852930.1: 126,802-170,063 , GRCh38.p12 chr7: 107,281,280-107,324,541	COG5
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
nsv7097101	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 107,188,536-107,204,434 , GRCh38.p12 chr7: 107,548,091-107,563,989 , GRCh38.p12 chr7\|NW_017852930.1: 393,746-409,644	COG5, DUS4L-BCAP29, 1 more genes
nsv6312518	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 107,204,228-107,204,434 , GRCh38.p12 chr7: 107,563,783-107,563,989 , GRCh38.p12 chr7\|NW_017852930.1: 409,438-409,644	COG5, DUS4L-BCAP29, 1 more genes
nsv4675258	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 106,596,321-106,910,550 , GRCh38.p12 chr7: 106,955,876-107,270,105	COG5, PRKAR2B-AS1, 2 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	COG5, GPR22, 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
nsv3896814	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 107,156,793-107,222,725 , GRCh38.p12 chr7\|NW_017852930.1: 362,003-427,935 , GRCh38.p12 chr7: 107,516,348-107,582,280	COG5, DUS4L-BCAP29, 2 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 42

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Number of Variants: 20

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Supplemental Content

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