dbVar for Gene (Select 6834) - 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
nsv4683889	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 135,771,850-137,038,881 , GRCh38.p12 chr9: 132,896,463-134,173,759	GBGT1, CELP, 46 more genes
nsv4681357	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 135,771,602-136,769,889 , GRCh38.p12 chr9: 132,896,215-133,904,767	ABO, GTF3C5, 40 more genes
nsv4614415	copy number variation	1	nstd183	human		GRCh37 chr9: 136,223,362-136,223,796 , GRCh38.p12 chr9: 133,356,486-133,356,920 , GRCh38.p12 chr9\|NW_009646201.1: 182,580-183,014	SURF2, SURF1
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
nsv4453311	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 134,379,574-138,678,377 , GRCh38.p12 chr9: 131,504,187-135,786,531	RNU6ATAC, RPL21P81, 114 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
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
nsv3918439	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 121,073,102-138,179,445 , GRCh37 chr9: 123,835,380-141,073,897 , NCBI36 chr9: 122,875,201-140,193,718	MIR4478, ENTR1, 498 more genes
nsv3917264	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 133,388,594-141,018,984 , NCBI36 chr9: 132,378,415-140,138,805 , GRCh38 chr9: 130,513,207-138,124,532	CFAP77, LINC01451, 253 more genes
nsv3917022	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 214,367-141,008,915 , GRCh38 chr9: 193,412-138,114,463 , NCBI36 chr9: 204,367-140,128,736	RN7SKP87, SPATA6L, 2168 more genes
nsv3916332	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 131,830,839-141,073,897 , GRCh38 chr9: 129,068,560-138,179,445 , NCBI36 chr9: 130,870,660-140,193,718	MIR3689D1, FIBCD1-AS1, 292 more genes
nsv3915973	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr9: 193,412-138,159,073 , GRCh37 chr9: 68,420,641-141,053,525 , NCBI36 chr9: 67,910,461-140,173,346	CTNNAL1, QSOX2, 2170 more genes
nsv3915923	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 121,684,719-140,132,214 , GRCh37.p13 chr9: 122,644,898-141,012,393 , GRCh38.p12 chr9: 119,882,620-138,117,941	NRARP, HMGA1P4, 511 more genes
nsv3915889	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 129,068,560-136,495,351 , NCBI36 chr9: 130,870,660-138,509,624 , GRCh37 chr9: 131,830,839-139,389,803	NTMT1, SLC2A6, 194 more genes

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Has Clinical Interpretation

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Items: 1 to 20 of 160

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Number of Variants: 20

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