plxnc1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3892486	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 94,541,920-94,543,958 , GRCh38.p12 chr12: 94,148,144-94,150,182	PLXNC1
nsv3904867	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 94,541,920-94,543,824 , GRCh38.p12 chr12: 94,148,144-94,150,048	PLXNC1
nsv3894042	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 94,541,920-94,543,411 , GRCh38.p12 chr12: 94,148,144-94,149,635	PLXNC1
nsv4456957	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 94,620,457-94,644,293 , GRCh38.p12 chr12: 94,226,681-94,250,517	PLXNC1
nsv5380743	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 94,634,261-94,806,266 , GRCh38.p12 chr12: 94,240,485-94,412,490	PLXNC1, CEP83, 1 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	PLXNC1, 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	PLXNC1, 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	PLXNC1, 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	PLXNC1, 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	PLXNC1, OR5BT1P, 2441 more genes
nsv3924338	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 89,962,226-108,055,398 , GRCh38 chr12: 91,044,318-109,133,210 , GRCh37 chr12: 91,438,095-109,571,015	PLXNC1, NUP37, 295 more genes
nsv3911770	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr12: 89,914,416-93,790,725 , GRCh37 chr12: 91,390,285-95,266,594 , GRCh38 chr12: 90,996,508-94,872,818	PLXNC1, BTG1, 63 more genes
nsv3895390	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr12: 94,091,911-94,619,578 , GRCh38.p12 chr12: 93,698,135-94,225,802	PLXNC1, CRADD, 7 more genes
nsv3904388	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 91,621,655-96,014,946 , GRCh38.p12 chr12: 91,227,878-95,621,170	PLXNC1, LOC100287148, 76 more genes
nsv4456428	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 94,090,866-94,616,552 , GRCh38.p12 chr12: 93,697,090-94,222,776	PLXNC1, CRADD, 7 more genes
nsv3921474	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr12: 93,374,113-94,267,175 , GRCh37 chr12: 93,767,889-94,660,951 , NCBI36 chr12: 92,292,020-93,185,082	PLXNC1, LOC643339, 16 more genes

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plxnc1[All Fields] AND 1[has_clinical] (17)
dbVar
txid398667[Organism:noexp] (3)
BioSample
ankyrin repeat domain-containing protein 2 isoform b [Homo sapiens]
ankyrin repeat domain-containing protein 2 isoform b [Homo sapiens]
gi|194018403|ref|NP_001123453.1|

Protein

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