galnt4[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
nsv3923771	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr12: 88,284,622-88,448,059 , GRCh37 chr12: 89,760,491-89,923,928 , GRCh38 chr12: 89,366,714-89,530,151	GALNT4, POC1B, 3 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	GALNT4, 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	GALNT4, MIR1252, 162 more genes
nsv4683190	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 88,910,111-89,985,072 , GRCh38.p12 chr12: 88,516,334-89,591,295	GALNT4, RNU1-117P, 15 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	GALNT4, 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	GALNT4, 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	GALNT4, 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	GALNT4, 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	GALNT4, OR5BT1P, 2441 more genes
nsv4578268	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr12: 87,296,336-90,301,051 , GRCh38.p12 chr12: 86,902,559-89,907,274	GALNT4, ATP2B1, 39 more genes
nsv6314102	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 89,546,727-89,911,511 , GRCh38.p12 chr12: 89,152,950-89,517,734	GALNT4, MRPS6P4, 6 more genes
nsv3906913	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 87,654,236-91,893,923 , GRCh38.p12 chr12: 87,260,459-91,500,146	GALNT4, ATP2B1, 53 more genes
nsv6309488	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 88,442,961-89,919,672 , GRCh38.p12 chr12: 88,049,184-89,525,895	GALNT4, RLIG1, 20 more genes

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