ccdc42[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 15

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3898050	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,241,916-8,692,213 , GRCh38.p12 chr17: 7,338,597-8,788,895	CCDC42, NDEL1, 108 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	CCDC42, MIR3185, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	CCDC42, P4HB, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	CCDC42, MIR21, 2366 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	CCDC42, SMURF2, 2366 more genes
nsv3897625	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 525-15,027,737 , GRCh38.p12 chr17: 150,732-15,124,420	CCDC42, GP1BA, 439 more genes
nsv3915354	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 150,732-14,764,202 , NCBI36 chr17: 525-14,608,244 , GRCh37 chr17: 525-14,667,519	CCDC42, KIF1C-AS1, 433 more genes
nsv3917059	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 45,835-12,247,218 , NCBI36 chr17: 11,807-12,187,943 , GRCh38 chr17: 162,016-12,343,901	CCDC42, PSMB6, 409 more genes
nsv7148254	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413	CCDC42, RFLNB, 401 more genes
nsv3904771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 525-11,186,432 , GRCh38.p12 chr17: 150,732-11,283,115	CCDC42, SLC2A4, 401 more genes
nsv3911050	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 5,732,953-12,095,349 , GRCh37 chr17: 5,636,273-11,998,666 , NCBI36 chr17: 5,576,997-11,939,391	CCDC42, C17orf49, 209 more genes
nsv3899694	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 7,431,013-9,868,179 , GRCh38.p12 chr17: 7,527,696-9,964,862	CCDC42, VAMP2, 109 more genes
nsv3902311	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 7,929,776-9,995,862 , GRCh38.p12 chr17: 8,026,458-10,092,545	CCDC42, RCVRN, 74 more genes
nsv3890702	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 8,219,814-8,676,240 , GRCh38.p12 chr17: 8,316,496-8,772,922	CCDC42, LOC105371530, 17 more genes
nsv3901829	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 8,412,394-8,729,543 , GRCh38.p12 chr17: 8,509,076-8,826,226	CCDC42, MFSD6L, 11 more genes

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ccdc42[All Fields] AND 1[has_clinical] (16)
dbVar
EDEM1 ER degradation enhancing alpha-mannosidase like protein 1 [Homo sapiens]
EDEM1 ER degradation enhancing alpha-mannosidase like protein 1 [Homo sapiens]
Gene ID:9695

Gene
Gene Links for GEO Profiles (Select 75923727) (1)
Gene
602424821F1 NIH_MGC_14 Homo sapiens cDNA clone IMAGE:4562789 5', mRNA sequence
602424821F1 NIH_MGC_14 Homo sapiens cDNA clone IMAGE:4562789 5', mRNA sequence
gi|13132482|gnl|dbEST|7990816|gb|BG 5.1|

Nucleotide

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