dbVar for Gene (Select 102467073) - 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
nsv7148204	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 9,999-14,320,000 , GRCh37.p13 chr5: 10,001-14,320,109	LOC105379638, LOC100420683, 185 more genes
nsv7144665	insertion	1	nstd232	human		GRCh37.p13 chr5: 271,937-271,937 , GRCh38.p12 chr5: 271,822-271,822	PDCD6, PDCD6-DT, 1 more genes
nsv7042391	inversion	1	nstd229	human		GRCh38 chr5: 190,811-661,964 , GRCh37.p13 chr5: 190,926-662,079	LOC100310782, LOC105374606, 20 more genes
nsv6776249	copy number variation	1	nstd229	human		GRCh38 chr5: 191,265-303,477 , GRCh37.p13 chr5: 191,380-303,592	CCDC127, LRRC14B, 5 more genes
nsv6772542	copy number variation	1	nstd229	human		GRCh38 chr5: 243,316-286,668 , GRCh37.p13 chr5: 243,431-286,783	PDCD6-AHRR, PPP4R2P1, 3 more genes
nsv6772296	copy number variation	1	nstd229	human		GRCh38 chr5: 105,167-310,399 , GRCh37.p13 chr5: 105,282-310,514	SDHA, PDCD6-DT, 6 more genes
nsv6771095	copy number variation	1	nstd229	human		GRCh38 chr5: 117,534-592,796 , GRCh37.p13 chr5: 117,649-592,911	SDHA, CCDC127, 17 more genes
nsv6770308	copy number variation	1	nstd229	human		GRCh38 chr5: 194,424-306,338 , GRCh37.p13 chr5: 194,539-306,453	CCDC127, LRRC14B, 5 more genes
nsv6765988	copy number variation	1	nstd229	human		GRCh38 chr5: 240,783-607,807 , GRCh37.p13 chr5: 240,898-607,922	LOC105374608, SDHA, 16 more genes
nsv6759682	copy number variation	1	nstd229	human		GRCh38 chr5: 151,928-460,171 , GRCh37.p13 chr5: 152,043-460,286	PDCD6-AHRR, EXOC3-AS1, 10 more genes
nsv6758743	copy number variation	1	nstd229	human		GRCh38 chr5: 224,651-375,400 , GRCh37.p13 chr5: 224,766-375,515	PPP4R2P1, PDCD6-AHRR, 4 more genes
nsv6637091	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 150,265-668,842 , GRCh38.p12 chr5: 150,150-668,727	EXOC3, SLC9A3, 21 more genes
nsv6636994	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 113,577-424,937 , GRCh38.p12 chr5: 113,462-424,822	AHRR, PDCD6-AHRR, 8 more genes
nsv6636942	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932	LOC105374608, LSP1P3, 351 more genes
nsv6636849	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-17,654,787 , GRCh38.p12 chr5: 113,462-17,654,678	ADCY2, HMGB3P3, 248 more genes
nsv6636672	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-26,164,852 , GRCh38.p12 chr5: 113,462-26,164,743	LINC02123, LINC01020, 302 more genes
nsv6636606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-31,448,527 , GRCh38.p12 chr5: 113,462-31,448,420	BASP1, RNU1-76P, 338 more genes
nsv6636438	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 113,577-316,451 , GRCh38.p12 chr5: 113,462-316,336	PLEKHG4B, SDHA, 6 more genes
nsv6636336	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 113,577-380,112 , GRCh38.p12 chr5: 113,462-379,997	SDHA, LRRC14B, 7 more genes
nsv6634383	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-2,027,194 , GRCh38.p12 chr5: 113,461-2,027,080	LINC02982, SLC12A7, 56 more genes

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Number of Variants: 20

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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

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Items: 1 to 20 of 374

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Number of Variants: 20

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