dbVar for Gene (Select 26493) - 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
nsv7137129	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659	VSIG10L2, OR8B6P, 268 more genes
nsv7077728	inversion	1	nstd229	human		GRCh38 chr11: 124,239,803-134,089,458 , GRCh37.p13 chr11: 124,110,545-133,959,353	LOC283172, PPP1R10P1, 175 more genes
nsv7064476	inversion	1	nstd229	human		GRCh38 chr11: 123,462,060-125,907,500 , GRCh37.p13 chr11: 123,332,768-125,777,395	STT3A, OR8G1, 101 more genes
nsv6898470	copy number variation	1	nstd229	human		GRCh38 chr11: 124,224,728-124,517,025 , GRCh37.p13 chr11: 124,095,433-124,386,921	OR8C1P, SLC5A4P1, 21 more genes
nsv6637558	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 122,975,824-134,938,470 , GRCh38.p12 chr11: 123,105,116-135,068,576	OR8B8, LOC107984373, 234 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	PYGM, ATL3, 2125 more genes
nsv6309036	copy number variation	3	nstd102	human	Uncertain significance	GRCh37 chr11: 123,504,851-126,163,012 , GRCh38.p12 chr11: 123,634,143-126,293,117	CDON, PKNOX2-DT, 113 more genes
nsv6291285	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 124,296,335-124,560,100 , GRCh38.p12 chr11: 124,426,439-124,690,204	OR8B8, SPA17, 12 more genes
nsv6291074	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847	ZW10, MPZL2, 378 more genes
nsv6289927	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522	IGSF9B, MIR10526, 592 more genes
nsv4981119	copy number variation	1	nstd200	human		GRCh38 chr11: 124,401,340-124,480,526 , GRCh37.p13 chr11: 124,271,236-124,350,422	OR8B8, OR8B9P, 5 more genes
nsv4844800	copy number variation	1	nstd200	human		GRCh37 chr11: 124,271,236-124,350,422 , GRCh38.p12 chr11: 124,401,340-124,480,526	OR8B8, OR8B9P, 5 more genes
nsv4732750	copy number variation	1	nstd199	human		GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572	, LINC02702, 392 more genes
nsv4675832	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 120,742,540-134,938,470 , GRCh38.p12 chr11: 120,871,831-135,068,576	MIR8052, BLID, 275 more genes
nsv4675674	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 124,232,608-134,938,470 , GRCh38.p12 chr11: 124,362,712-135,068,576	FAM118B, PUS3, 184 more genes
nsv4674572	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571	ACRV1, APLP2, 382 more genes
nsv4673961	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 124,226,940-134,944,477 , GRCh38.p12 chr11: 124,357,044-135,074,583	OR8A2P, LOC101929473, 186 more genes
nsv4455281	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 117,830,263-134,938,470 , GRCh38.p12 chr11: 117,959,548-135,068,576	NTM-AS1, LOC403312, 369 more genes
nsv4436748	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 120,576,984-134,934,063 , GRCh38.p12 chr11: 120,706,275-135,064,169	LINC02098, LOC105369587, 276 more genes
nsv4349506	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 116,691,675-134,889,485 , GRCh38.p12 chr11: 116,820,959-135,019,591	LOC107984407, DCPS, 394 more genes

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 154

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Number of Variants: 20

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