rxylt1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv7093310	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 64,173,474-64,173,889 , GRCh38 chr12: 63,779,694-63,780,109	RXYLT1
nsv3889865	copy number variation	2	nstd102	human	Uncertain significance	GRCh38 chr12: 63,805,214-63,805,424 , GRCh37 chr12: 64,198,994-64,199,204	RXYLT1
nsv7094219	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 64,199,004-64,199,194 , GRCh38.p12 chr12: 63,805,224-63,805,414	RXYLT1
nsv7094152	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 64,198,994-64,238,683 , GRCh38.p12 chr12: 63,805,214-63,844,903	RXYLT1, SRGAP1, 3 more genes
nsv3916302	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 59,587,199-65,248,124 , GRCh37 chr12: 61,300,932-66,961,857 , GRCh38 chr12: 60,907,151-66,568,077	RXYLT1, LOC105369809, 93 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	RXYLT1, 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	RXYLT1, 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	RXYLT1, 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	RXYLT1, 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	RXYLT1, OR5BT1P, 2441 more genes
nsv4681587	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 64,173,731-64,895,171 , GRCh38.p12 chr12: 63,779,951-64,501,391	RXYLT1, XPOT, 16 more genes
nsv3912443	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr12: 62,081,713-62,638,706 , GRCh37.p13 chr12: 63,795,446-64,352,439 , GRCh38.p12 chr12: 63,401,666-63,958,659	RXYLT1, MIR10527, 10 more genes

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rxylt1[All Fields] AND 1[has_clinical] (13)
dbVar
Sdc[All Fields] AND 1[has_clinical] (27)
dbVar
nuclear migration protein nudC [Drosophila sechellia]
nuclear migration protein nudC [Drosophila sechellia]
gi|195328242|ref|XP_002030825.1|

Protein

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