ccdc59[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 13

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3923301	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr12: 81,101,681-81,370,089 , GRCh37.p13 chr12: 82,577,550-82,845,958 , GRCh38.p12 chr12: 82,183,771-82,452,179	CCDC59, LOC105369873, 1 more genes
nsv3892030	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 69,608,090-89,629,345 , GRCh38.p12 chr12: 69,214,310-89,235,568	CCDC59, LOC101928002, 197 more genes
nsv3922777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 73,879,477-93,189,581 , NCBI36 chr12: 72,165,744-91,713,712 , GRCh38 chr12: 73,485,697-92,795,805	CCDC59, RN7SL734P, 195 more genes
nsv4456763	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 77,737,623-94,330,526 , GRCh38.p12 chr12: 77,343,843-93,936,750	CCDC59, MIR1252, 162 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	CCDC59, RNA5SP369, 2454 more genes
nsv3905447	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316	CCDC59, LOH12CR2, 2452 more genes
nsv3897722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059	CCDC59, RNU4ATAC16P, 2452 more genes
nsv3914194	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807	CCDC59, BTG1P1, 2451 more genes
nsv3904719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532	CCDC59, OR5BT1P, 2441 more genes
nsv3914424	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 76,482,668-84,288,731 , GRCh38 chr12: 77,564,757-85,370,822 , GRCh37 chr12: 77,958,537-85,764,600	CCDC59, LOC105369875, 59 more genes
nsv4348838	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 82,183,041-88,755,577 , GRCh38.p12 chr12: 81,789,262-88,361,800	CCDC59, LOC101059974, 47 more genes
nsv3896674	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 82,315,146-83,005,702 , GRCh38.p12 chr12: 81,921,367-82,611,923	CCDC59, LOC100418732, 5 more genes
nsv3900140	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 81,666,797-82,808,748 , GRCh38.p12 chr12: 81,273,018-82,414,969	CCDC59, LOC105369872, 6 more genes

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ccdc59[All Fields] AND 1[has_clinical] (14)
dbVar
Homo sapiens TIMP metallopeptidase inhibitor 1 (TIMP1), mRNA
Homo sapiens TIMP metallopeptidase inhibitor 1 (TIMP1), mRNA
gi|73858576|ref|NM_003254.2|

Nucleotide

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