arb2a[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3911866	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 93,080,814-93,293,032 , GRCh37 chr5: 93,055,058-93,267,276 , GRCh38 chr5: 93,719,352-93,931,571	ARB2A, POU5F2
nsv4729486	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 93,065,634-93,132,679 , GRCh38.p12 chr5: 93,729,928-93,796,973	ARB2A, POU5F2
nsv6314498	complex chromosomal rearrangement	5	nstd102	human	Pathogenic	GRCh37 chr5: 93,026,965-93,026,965 , GRCh37 chr5: 93,258,066-93,258,066 , GRCh37 chr5: 153,852,297-153,852,297 , GRCh37 chr5: 153,351,885-153,351,885 , GRCh37 chr5: 153,351,885-153,351,885 , GRCh37 chr5: 153,852,297-153,852,297 , GRCh37 chr5: 93,026,965-93,026,965 , GRCh37 chr5: 92,616,397-92,616,397 , GRCh37 chr5: 92,616,397-92,616,397 , GRCh37 chr5: 93,258,062-93,258,062 , GRCh38.p12 chr5: 93,691,259-93,691,259 , GRCh38.p12 chr5: 154,472,737-154,472,737 , GRCh38.p12 chr5: 93,922,357-93,922,357 , GRCh38.p12 chr5: 153,972,325-153,972,325 , GRCh38.p12 chr5: 93,691,259-93,691,259 , GRCh38.p12 chr5: 93,922,361-93,922,361 , GRCh38.p12 chr5: 93,280,691-93,280,691 , GRCh38.p12 chr5: 93,280,691-93,280,691 , GRCh38.p12 chr5: 153,972,325-153,972,325 , GRCh38.p12 chr5: 154,472,737-154,472,737	ARB2A, LOC107983980, 1 more genes
nsv6291217	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 92,986,133-93,167,165 , GRCh38.p12 chr5: 93,650,427-93,831,459	ARB2A, NPM1P27, 1 more genes
nsv3915936	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 93,416,111-93,588,509 , GRCh38 chr5: 94,080,406-94,252,804 , NCBI36 chr5: 93,441,867-93,614,265	ARB2A, KIAA0825, 1 more genes
nsv3923406	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 92,959,705-93,599,283 , GRCh37 chr5: 92,933,949-93,573,527 , GRCh38 chr5: 93,598,243-94,237,822	ARB2A, POU5F2, 4 more genes
nsv4675441	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 92,618,672-93,196,696 , GRCh38.p12 chr5: 93,282,966-93,860,990	ARB2A, NR2F1, 4 more genes
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	ARB2A, MEGF10, 2080 more genes
nsv3884357	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 86,400,000-154,000,000 , GRCh38.p12 chr5: 87,104,183-154,620,440	ARB2A, TXNDC15, 962 more genes
nsv3915450	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 90,707,525-130,655,256 , NCBI36 chr5: 90,743,281-130,683,155 , GRCh38 chr5: 91,411,708-131,319,563	ARB2A, MCTP1, 422 more genes
nsv3916468	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 89,670,423-127,412,115 , GRCh38 chr5: 90,374,606-128,076,423 , NCBI36 chr5: 89,706,179-127,440,014	ARB2A, LOC105379149, 406 more genes
nsv3924896	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 84,603,580-111,435,081 , GRCh37 chr5: 83,899,398-110,770,779 , NCBI36 chr5: 83,935,154-110,798,678	ARB2A, LOC107986438, 254 more genes
nsv3920768	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 92,235,441-118,949,814 , GRCh38 chr5: 92,899,734-119,614,119 , NCBI36 chr5: 92,261,197-118,977,713	ARB2A, LOC102724720, 292 more genes
nsv3921006	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 92,554,566-112,651,391 , GRCh37 chr5: 92,528,810-112,623,492 , GRCh38 chr5: 93,193,104-113,287,795	ARB2A, FBXL17, 204 more genes
nsv3914008	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 88,377,169-104,022,949 , NCBI36 chr5: 88,412,925-104,050,848 , GRCh38 chr5: 89,081,352-104,687,248	ARB2A, LOC105379080, 166 more genes
nsv3921368	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 86,672,700-100,860,147 , NCBI36 chr5: 86,708,456-100,888,046 , GRCh38 chr5: 87,376,883-101,524,443	ARB2A, LOC107986438, 158 more genes
nsv3879974	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 91,504,101-104,858,348 , GRCh38.p12 chr5: 92,208,284-105,522,647	ARB2A, LOC105379090, 142 more genes
nsv3874231	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 87,512,314-95,096,562 , GRCh38.p12 chr5: 88,216,497-95,760,858	ARB2A, ARRDC3, 71 more genes
nsv3912526	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 91,386,552-98,365,880 , NCBI36 chr5: 90,718,125-97,729,488 , GRCh37 chr5: 90,682,369-97,701,584	ARB2A, RTRAFP2, 77 more genes
nsv7148188	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 88,189,536-93,784,597 , GRCh37.p13 chr5: 87,485,353-93,120,303	ARB2A, RPS3AP22, 49 more genes

dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Send to:

Search results

Items: 1 to 20 of 39

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 39

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity