dbVar for Gene (Select 55572) - 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
nsv5647743	insertion	1	nstd207	human		GRCh38 chr11: 126,276,308-126,276,308 , GRCh37.p13 chr11: 126,146,203-126,146,203	FOXRED1, RPL35AP26
nsv4750342	insertion	1	nstd199	human		GRCh37 chr11: 126,146,199-126,146,199 , GRCh38.p12 chr11: 126,276,304-126,276,304	FOXRED1, RPL35AP26
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
nsv4728891	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 125,785,487-134,938,470 , GRCh38.p12 chr11: 125,915,592-135,068,576	ARHGAP32, NAP1L1P1, 125 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
nsv4456524	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 126,111,090-127,755,537 , GRCh38.p12 chr11: 126,241,195-127,885,642	LOC107984379, RPL35AP26, 23 more genes
nsv4455981	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 125,661,975-126,610,328 , GRCh38.p12 chr11: 125,792,080-126,740,433	RN7SL351P, NAP1L1P1, 23 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
nsv4448148	insertion	1	nstd175	human		GRCh37 chr11: 126,146,203-126,146,203 , GRCh38.p12 chr11: 126,276,308-126,276,308	FOXRED1, RPL35AP26
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
nsv4350042	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 125,446,101-134,904,063 , GRCh38.p12 chr11: 125,576,205-135,034,169	SNX19, TP53AIP1, 138 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
nsv4349045	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 116,700,253-134,904,063 , GRCh38.p12 chr11: 116,829,537-135,034,169	MPZL3, ADAMTS8, 393 more genes
nsv4210792	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 126,134,000-126,145,000 , GRCh38.p12 chr11: 126,264,105-126,275,105	FOXRED1, FAM118B, 1 more genes
nsv3967730	insertion	1	nstd168	human		GRCh38 chr11: 126,222,213-126,280,185 , GRCh37.p13 chr11: 126,092,108-126,150,080	SRPRA, FOXRED1, 3 more genes
nsv3946786	insertion	1	nstd167	human		GRCh37 chr11: 126,146,203-126,146,203 , GRCh38.p12 chr11: 126,276,308-126,276,308	FOXRED1, RPL35AP26
nsv3924932	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 125,761,210-128,942,286 , GRCh38 chr11: 125,891,315-129,072,391 , NCBI36 chr11: 125,266,420-128,447,496	KCNJ1, LOC107984409, 52 more genes

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Number of Variants: 20

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 192

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Number of Variants: 20

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