dbVar for Gene (Select 100128893) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5023997	copy number variation	1	nstd200	human		GRCh38 chr18: 22,116,636-22,169,182 , GRCh37.p13 chr18: 19,696,597-19,749,143	GATA6-AS1, RNU6ATAC20P, 1 more genes
nsv5023996	copy number variation	1	nstd200	human		GRCh38 chr18: 22,048,064-24,963,279 , GRCh37.p13 chr18: 19,628,025-22,543,243	, LOC105372028, 47 more genes
nsv4682554	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 19,748,323-19,752,250 , GRCh38.p12 chr18: 22,168,362-22,172,289	GATA6, GATA6-AS1
nsv3924706	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097	LOC100420948, NPM1P2, 941 more genes
nsv3924638	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 20,962,119-74,691,446 , NCBI36 chr18: 16,796,078-70,532,390 , GRCh37 chr18: 18,542,080-72,403,402	HMGN1P30, LOC107985134, 596 more genes
nsv3924351	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 108,760-76,113,817 , GRCh38 chr18: 118,760-80,254,946 , GRCh37 chr18: 118,760-78,012,829	MIX23P1, LOC105372087, 942 more genes
nsv3923838	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 138,963-76,103,255 , GRCh37 chr18: 148,963-78,002,264 , GRCh38 chr18: 148,963-80,244,381	WDR7-OT1, HMGN1P30, 941 more genes
nsv3921458	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 13,330,111-19,243,841 , GRCh37 chr18: 13,340,111-20,989,843 , GRCh38 chr18: 13,340,112-23,409,879	TERF1P2, RPL34P32, 97 more genes
nsv3920818	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 15,370,696-76,117,153 , GRCh37.p13 chr18: 15,380,696-78,016,181 , GRCh38.p12 chr18: 15,380,697-80,258,298	AQP4-AS1, SERPINB8, 670 more genes
nsv3920487	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 16,783,337-30,197,417 , GRCh38 chr18: 20,949,378-34,363,455 , GRCh37 chr18: 18,529,339-31,943,419	CCDC178, RNA5SP452, 159 more genes
nsv3919004	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 136,226-80,256,240 , GRCh37 chr18: 136,226-78,014,123 , NCBI36 chr18: 126,226-76,115,097	LIVAR, LINC03069, 941 more genes
nsv3918488	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 43,345-76,068,860 , GRCh38 chr18: 53,345-80,209,986 , GRCh37 chr18: 53,345-77,967,869	LOC105372027, ASXL3, 945 more genes
nsv3916426	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 149,089-77,992,274 , NCBI36 chr18: 139,089-76,093,265 , GRCh38 chr18: 149,089-80,234,391	TPGS2, TWSG1-DT, 941 more genes
nsv3916358	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 20,941,324-40,360,620 , NCBI36 chr18: 16,775,283-36,194,582 , GRCh37 chr18: 18,521,285-37,940,584	MIR4741, LOC105372029, 220 more genes
nsv3915938	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 18,569,723-77,967,869 , GRCh38 chr18: 20,989,762-80,209,986 , NCBI36 chr18: 16,823,721-76,068,860	LOC105372061, LOC107985171, 670 more genes
nsv3914075	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 18,540,281-26,181,841 , NCBI36 chr18: 16,794,279-24,435,839 , GRCh38 chr18: 20,960,320-28,601,877	LINC01900, HRH4, 106 more genes
nsv3913178	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 8,779,843-24,685,379 , GRCh37 chr18: 8,779,841-22,265,343 , NCBI36 chr18: 8,769,841-20,519,341	RN7SL745P, LOC105372017, 211 more genes
nsv3912925	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr18: 138,963-76,111,023 , GRCh38 chr18: 148,963-80,252,149 , GRCh37 chr18: 148,963-78,010,032	LOC105372038, RN7SKP182, 941 more genes
nsv3911404	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 16,794,279-76,093,303 , GRCh38 chr18: 20,960,320-80,234,429 , GRCh37 chr18: 18,540,281-77,992,312	LOC107985178, RN7SL310P, 670 more genes
nsv3910887	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr18: 139,089-76,113,807 , GRCh37 chr18: 149,089-78,012,819 , GRCh38 chr18: 149,089-80,254,936	LPIN2, RNU6-408P, 941 more genes

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Number of Variants: 20

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Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 145

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Number of Variants: 20

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