ccdc105[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
nsv3909889	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 14,126,774-16,886,123 , GRCh38 chr19: 14,154,962-16,914,313 , GRCh37 chr19: 14,265,774-17,025,123	OR7A1P, SNRPGP15, 108 more genes
nsv3908579	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 14,124,666-16,431,349 , GRCh38.p12 chr19: 14,013,854-16,320,538	TMEM167AP2, TEKTL1, 99 more genes
nsv3899292	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 14,883,158-16,788,770 , GRCh38.p12 chr19: 14,772,346-16,677,959	KLF2, ADGRE2, 80 more genes
nsv3910509	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 13,505,739-15,342,900 , GRCh37 chr19: 13,644,739-15,481,900 , GRCh38 chr19: 13,533,925-15,371,089	DDX39A, SLC1A6, 76 more genes
nsv4676112	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 14,368,330-15,712,368 , GRCh38.p12 chr19: 14,257,518-15,601,557	GIPC1, LOC100422106, 52 more genes
nsv7098925	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 15,014,099-16,261,691 , GRCh37.p13 chr19: 15,124,911-16,372,502	CYP4F12, OR1AB1P, 52 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	ZNF321P, ZNF861P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	BABAM1, BEST2, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	LENG8, SYDE1, 2408 more genes
nsv3913730	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354	BCKDHA, ADGRE5, 1102 more genes
nsv3922457	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 14,085,489-28,330,584 , GRCh38 chr19: 13,974,677-27,839,676 , NCBI36 chr19: 13,946,489-33,022,424	REX1BD, ZNF92P2, 416 more genes
nsv4729750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 14,286,624-20,956,753 , GRCh38.p12 chr19: 14,175,812-20,773,947	LOC105372309, RAB8A, 269 more genes
nsv7095645	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 14,847,048-17,394,124 , GRCh38.p12 chr19: 14,736,236-17,283,315	HAUS8, MIR1470, 95 more genes
nsv3910299	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 14,517,721-15,521,581 , GRCh38 chr19: 14,406,909-15,410,770 , NCBI36 chr19: 14,378,721-15,382,581	EPHX3, SNORA104, 43 more genes
nsv3910918	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 14,588,573-15,244,464 , NCBI36 chr19: 14,449,573-15,105,464 , GRCh38 chr19: 14,477,761-15,133,653	GIPC1, TECR, 31 more genes

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ccdc105[All Fields] AND 1[has_clinical] (16)
dbVar
Dysomma anguillare[orgn] (26)
Nucleotide
RNA for Nucleotide (Select 568215752) (10)
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