dbVar for Gene (Select 440132) - 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
nsv6112810	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 28,925,153-34,061,696 , GRCh38.p12 chr13: 28,351,016-33,487,559	MTUS2, ALOX5AP, 70 more genes
nsv5564510	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053	RN7SL272P, DIAPH3, 1333 more genes
nsv5511667	copy number variation	1	nstd206	human		GRCh38 chr13: 30,880,951-30,882,715 , GRCh37.p13 chr13: 31,455,088-31,456,852	LINC00545, TEX26-AS1
nsv4996803	copy number variation	1	nstd200	human		GRCh38 chr13: 30,880,951-30,882,715 , GRCh37.p13 chr13: 31,455,088-31,456,852	TEX26-AS1, LINC00545
nsv3924676	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 18,456,040-114,340,285 , GRCh37 chr13: 19,030,180-115,105,760 , NCBI36 chr13: 17,928,180-114,123,862	GRTP1, FABP5P1, 1334 more genes
nsv3924246	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 29,785,946-38,739,818 , GRCh37 chr13: 30,887,946-39,841,818 , GRCh38 chr13: 30,313,809-39,267,681	LINC01048, N4BP2L2-IT2, 117 more genes
nsv3923402	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 30,228,271-33,432,383 , GRCh38 chr13: 29,654,134-32,858,245 , NCBI36 chr13: 29,126,271-32,330,383	RXFP2, LINC00572, 53 more genes
nsv3922472	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 28,793,591-36,467,485 , GRCh38 chr13: 29,321,454-36,995,348 , GRCh37 chr13: 29,895,591-37,569,485	LINC00445, CCDC169, 103 more genes
nsv3922463	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 18,418,322-114,088,205 , GRCh37 chr13: 19,520,322-115,070,103 , GRCh38 chr13: 18,946,182-114,304,628	TULP3P1, LOC105370349, 1311 more genes
nsv3921223	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 19,671,934-114,340,331 , NCBI36 chr13: 19,144,074-114,123,908 , GRCh37 chr13: 20,246,074-115,085,141	TRIM60P13, LINC00351, 1289 more genes
nsv3920749	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 20,407,270-115,064,089 , GRCh38 chr13: 19,833,130-114,298,614 , NCBI36 chr13: 19,305,270-114,082,191	DIAPH3-AS2, LOC105370216, 1281 more genes
nsv3920559	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 29,647,457-37,130,151 , NCBI36 chr13: 28,545,457-36,028,151 , GRCh38 chr13: 29,073,320-36,556,014	LINC02343, N4BP2L2, 92 more genes
nsv3919574	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 18,850,545-114,327,173 , GRCh37 chr13: 19,296,527-115,085,141 , NCBI36 chr13: 18,194,527-114,110,750	RNU6-77P, LINC00457, 1317 more genes
nsv3917322	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr13: 19,309,535-114,110,750 , GRCh37 chr13: 20,411,535-115,085,141 , GRCh38 chr13: 19,837,395-114,327,173	RNY1P7, LINC01039, 1283 more genes
nsv3916629	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,139,188-115,085,141 , NCBI36 chr13: 18,037,188-114,110,750 , GRCh38 chr13: 18,565,048-114,327,173	TM9SF2, LOC107984564, 1330 more genes
nsv3916116	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 19,305,270-114,110,683 , GRCh38 chr13: 19,833,130-114,327,106 , GRCh37 chr13: 20,407,270-115,085,141	LOC105370263, RPS7P10, 1283 more genes
nsv3915833	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,532,231-31,664,597 , GRCh38 chr13: 18,958,091-31,090,460 , NCBI36 chr13: 18,430,231-30,562,597	PPIAP28, RNY3P4, 261 more genes
nsv3915679	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 31,271,865-70,046,105 , GRCh38 chr13: 30,697,728-69,471,973 , NCBI36 chr13: 30,169,865-68,944,106	CCDC70, ZC3H13, 524 more genes
nsv3914899	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 19,436,286-115,107,733 , GRCh38 chr13: 18,862,146-114,342,258 , NCBI36 chr13: 18,334,286-114,125,835	EFNB2, SNORA27, 1319 more genes
nsv3911871	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 19,671,934-40,914,767 , NCBI36 chr13: 19,144,074-40,386,903 , GRCh37 chr13: 20,246,074-41,488,903	LOC105370152, PCOTHP1, 362 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Study Type

Subject Phenotype Status

Additional filters

Links from Gene

Items: 1 to 20 of 87

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Number of Variants: 20

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