iscu[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
nsv7093952	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 108,956,399-108,962,692 , GRCh38.p12 chr12: 108,562,623-108,568,916	ISCU
nsv6291583	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 104,230,462-111,984,801 , GRCh38.p12 chr12: 103,836,684-111,546,997	ISCU, LOC105369964, 147 more genes
nsv3916234	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 104,152,585-111,116,873 , GRCh37 chr12: 105,628,455-112,632,490 , GRCh38 chr12: 105,234,677-112,194,686	ISCU, LOC100287944, 141 more genes
nsv4728881	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 106,498,814-112,252,906 , GRCh38.p12 chr12: 106,105,036-111,815,102	ISCU, ATP2A2, 115 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	ISCU, 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	ISCU, 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	ISCU, 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	ISCU, 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	ISCU, 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	ISCU, NUP37, 295 more genes
nsv3893927	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr12: 103,044,333-111,639,805 , GRCh38.p12 chr12: 102,650,555-111,202,001	ISCU, ACACB, 150 more genes
nsv3919676	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr12: 104,562,875-107,917,026 , GRCh37 chr12: 106,038,745-109,432,645 , GRCh38 chr12: 105,644,967-108,994,840	ISCU, SELPLG, 54 more genes
nsv4769383	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 107,197,584-109,830,564 , GRCh38.p12 chr12: 106,803,806-109,392,759	ISCU, TMEM263, 50 more genes
nsv3922307	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr12: 107,235,550-107,537,319 , GRCh37.p13 chr12: 108,711,420-109,013,190 , GRCh38.p12 chr12: 108,317,643-108,619,414	ISCU, FICD, 4 more genes
nsv7137136	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 108,917,234-109,052,695 , GRCh38.p12 chr12: 108,523,457-108,658,919	ISCU, TMEM119, 5 more genes

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iscu[All Fields] AND 1[has_clinical] (16)
dbVar
FAM168B family with sequence similarity 168 member B [Homo sapiens]
FAM168B family with sequence similarity 168 member B [Homo sapiens]
Gene ID:130074

Gene
DELEC1 deleted in esophageal cancer 1 [Homo sapiens]
DELEC1 deleted in esophageal cancer 1 [Homo sapiens]
Gene ID:50514

Gene

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