dbVar for Gene (Select 22845) - 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
nsv5304476	copy number variation	1	nstd204	human		GRCh37.p13 chr9: 131,694,758-131,726,143 , GRCh38.p13 chr9: 128,932,479-128,963,864	DOLK, NUP188, 1 more genes
nsv5248733	copy number variation	1	nstd204	human		GRCh38.p13 chr9: 128,932,201-128,963,900 , GRCh37.p13 chr9: 131,694,480-131,726,179	DOLK, PHYHD1, 1 more genes
nsv5241889	copy number variation	1	nstd204	human		GRCh38.p13 chr9: 128,441,101-129,240,100 , GRCh37.p13 chr9: 131,203,380-132,002,379	, KYAT1, 32 more genes
nsv4985753	copy number variation	1	nstd200	human		GRCh38 chr9: 128,935,330-128,951,137 , GRCh37.p13 chr9: 131,697,609-131,713,416	NUP188, PHYHD1, 1 more genes
nsv4769385	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 131,282,528-131,720,659 , GRCh38.p12 chr9: 128,520,249-128,958,380	LOC101929270, TBC1D13, 20 more genes
nsv4682405	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 131,707,956-131,709,592 , GRCh38.p12 chr9: 128,945,677-128,947,313	DOLK, NUP188
nsv4675731	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,957,344-132,310,210 , GRCh38.p12 chr9: 128,195,065-129,547,931	PTPA, GLE1, 55 more genes
nsv4675555	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 131,094,304-131,863,858 , GRCh38.p12 chr9: 128,332,025-129,101,579	ENDOG, SPOUT1, 35 more genes
nsv4457273	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936	CDRT15P14, MIR548AW, 2167 more genes
nsv4455186	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937	LOC105376327, ENG, 1304 more genes
nsv4349353	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr9: 131,670,024-134,514,071 , GRCh38.p12 chr9: 128,907,745-131,638,684	ABL1, ASS1, 69 more genes
nsv4337085	sequence alteration	1	nstd166	human		GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042	, ABCA1, 927 more genes
nsv3957444	copy number variation	1	nstd168	human		GRCh38 chr9: 128,916,116-128,945,598 , GRCh37.p13 chr9: 131,678,395-131,707,877	DOLK, LRRC8A, 2 more genes
nsv3923672	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 130,681,755-132,842,253 , GRCh38 chr9: 127,919,476-130,079,974 , NCBI36 chr9: 129,721,576-131,882,074	PIP5KL1, NTMT1, 80 more genes
nsv3922684	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897	TDRD7, CDK9, 2170 more genes
nsv3921598	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389	PGAP4, ECPAS, 2167 more genes
nsv3920829	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 121,112,395-138,075,224 , GRCh37 chr9: 123,874,673-140,969,676 , NCBI36 chr9: 122,914,494-140,089,497	LOC101928786, NRON, 495 more genes
nsv3920713	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 193,862-140,140,210 , GRCh38 chr9: 203,862-138,125,937 , GRCh37 chr9: 203,862-141,020,389	ABHD17B, LOC100533707, 2167 more genes
nsv3919948	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 125,554,937-141,018,984 , GRCh38 chr9: 122,792,658-138,124,532 , NCBI36 chr9: 124,594,758-140,138,805	LOC107987143, ATP6V1G1P3, 456 more genes
nsv3919257	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 204,193-141,073,897 , GRCh38 chr9: 204,193-138,179,445 , NCBI36 chr9: 194,193-140,193,718	LOC107987031, LOC105376234, 2169 more genes

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Number of Variants: 20

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