dbVar for Gene (Select 84837) - 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
nsv4685750	copy number variation	1	nstd102	human	not provided	GRCh37 chr14: 20,511,672-42,881,888 , GRCh38.p12 chr14: 20,043,513-42,412,685	IGBP1P1, RAB2B, 579 more genes
nsv4680310	copy number variation	1	nstd189	human		GRCh37.p13 chr14: 32,117,530-32,594,300 , GRCh38.p12 chr14: 31,648,324-32,125,094	ARHGAP5, NUBPL, 5 more genes
nsv4676015	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 32,110,535-32,603,615 , GRCh38.p12 chr14: 31,641,329-32,134,409	RNU6-602P, LINC02313, 5 more genes
nsv4675943	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,672-44,829,030 , GRCh38.p12 chr14: 20,043,513-44,359,827	TRAJ36, SEC23A-AS1, 590 more genes
nsv4630752	copy number variation	1	nstd183	human		GRCh37 chr14: 31,954,081-32,599,329 , GRCh38.p12 chr14: 31,484,875-32,130,123	LOC105370440, NUBPL-DT, 8 more genes
nsv4529189	copy number variation	1	nstd166	human		GRCh37.p13 chr14: 32,232,999-32,571,000 , GRCh38.p12 chr14: 31,763,793-32,101,794	NUBPL, ARHGAP5-AS1, 3 more genes
nsv4457320	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 30,448,939-35,017,859 , GRCh38.p12 chr14: 29,979,733-34,548,653	NARS1P1, RNU1-27P, 56 more genes
nsv4456831	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 32,110,535-32,603,600 , GRCh38.p12 chr14: 31,641,329-32,134,394	NUBPL, RNU6-602P, 5 more genes
nsv4455999	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 32,110,535-32,600,382 , GRCh38.p12 chr14: 31,641,329-32,131,176	LOC105370440, ARHGAP5-AS1, 5 more genes
nsv4455578	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 32,464,298-32,767,649 , GRCh38.p12 chr14: 31,995,092-32,298,443	ARHGAP5-AS1, LOC100533787, 6 more genes
nsv4415453	copy number variation	1	nstd174	human		GRCh37 chr14: 31,958,566-32,584,337 , GRCh38.p12 chr14: 31,489,360-32,115,131	ARHGAP5, NUBPL, 7 more genes
nsv4224354	copy number variation	1	nstd166	human		GRCh37.p13 chr14: 32,542,447-32,545,670 , GRCh38.p12 chr14: 32,073,241-32,076,464	ARHGAP5, ARHGAP5-AS1
nsv3924751	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 31,261,477-45,154,334 , GRCh38 chr14: 30,792,271-44,685,131 , NCBI36 chr14: 30,331,228-44,224,084	DNAJC8P1, SNORA101B, 171 more genes
nsv3922917	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 30,851,760-38,181,546 , NCBI36 chr14: 29,921,511-37,251,297 , GRCh38 chr14: 30,382,554-37,712,341	MBIP, LOC105370447, 124 more genes
nsv3922163	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr14: 26,243,854-32,957,356 , GRCh37.p13 chr14: 27,174,014-33,887,605 , GRCh38.p12 chr14: 26,704,808-33,418,399	LINC02293, ARHGAP5, 77 more genes
nsv3919106	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482	SRMP2, IGHV3-71, 1929 more genes
nsv3918965	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,490,852-44,562,875 , GRCh38 chr14: 20,022,693-44,093,672 , NCBI36 chr14: 19,560,692-43,632,625	TRAJ13, LRP10, 589 more genes
nsv3917583	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr14: 31,165,713-31,685,490 , GRCh37.p13 chr14: 32,095,962-32,615,739 , GRCh38.p12 chr14: 31,626,756-32,146,533	ARHGAP5-AS1, ARHGAP5, 5 more genes
nsv3917422	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478	MIR656, TRAJ59, 1918 more genes
nsv3917157	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 24,018,169-42,452,605 , GRCh38 chr14: 23,548,960-41,983,402 , NCBI36 chr14: 23,088,009-41,522,355	LINC02300, COCH, 274 more genes

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Number of Variants: 20

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dbVar

Result Filters

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Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

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Subject Phenotype Status

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Items: 1 to 20 of 84

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Number of Variants: 20

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