U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 105

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5023590copy number variation1nstd200human GRCh38 chr17: 5,094,869-5,399,676 , GRCh37.p13 chr17: 4,998,164-5,302,996 LOC105371505, ZNF232-AS1, 8 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4674912copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-5,627,408 , GRCh38.p12 chr17: 158,756-5,724,088 SRR, DBIL5P, 196 more genes
    nsv4630208copy number variation1nstd183human GRCh37 chr17: 4,486,568-5,620,052 , GRCh38.p12 chr17: 4,583,273-5,716,732 , ARRB2, 59 more genes
    nsv4457731copy number variation1nstd102humanUncertain significance GRCh37 chr17: 4,845,435-5,097,302 , GRCh38.p12 chr17: 4,942,140-5,194,007 ZNF594, ZNF232, 18 more genes
    nsv4457587copy number variation1nstd102humanUncertain significance GRCh37 chr17: 3,759,126-6,128,911 , GRCh38.p12 chr17: 3,855,832-6,225,591 DERL2, ZZEF1, 82 more genes
    nsv4350781copy number variation1nstd102humanPathogenic GRCh37 chr17: 47,546-6,287,620 , GRCh38.p12 chr17: 197,755-6,384,300 SERPINF1, UBE2G1, 201 more genes
    nsv3923881copy number variation1nstd102humanPathogenic NCBI36 chr17: 48,539-4,989,051 , GRCh37.p13 chr17: 48,539-5,048,327 , GRCh38.p12 chr17: 198,748-5,145,032 CAMKK1, MIR6776, 177 more genes
    nsv3923152copy number variation1nstd102humanPathogenic NCBI36 chr17: 3,451,558-7,022,067 , GRCh38 chr17: 3,601,515-7,178,024 , GRCh37 chr17: 3,504,809-7,081,343 PSMB6, NUP88, 133 more genes
    nsv3922546copy number variation1nstd102humanPathogenic NCBI36 chr17: 525-5,779,421 , GRCh38 chr17: 150,732-5,935,377 , GRCh37 chr17: 525-5,838,697 CHRNE, SPNS2-AS1, 198 more genes
    nsv3920795copy number variation1nstd102humanPathogenic GRCh38 chr17: 2,062,380-5,258,340 , NCBI36 chr17: 1,912,424-5,102,359 , GRCh37 chr17: 1,965,674-5,161,635 LINC01996, OR3A1, 128 more genes
    nsv3919907copy number variation1nstd102humanLikely benign GRCh38 chr17: 4,092,608-5,354,473 , GRCh37 chr17: 3,995,902-5,257,768 , NCBI36 chr17: 3,942,651-5,198,492 RPS12P29, RN7SL774P, 59 more genes
    nsv3917777copy number variation1nstd102humanPathogenic GRCh37 chr17: 50,690-7,394,448 , GRCh38 chr17: 198,748-7,491,129 , NCBI36 chr17: 48,539-7,335,172 PAFAH1B1, PELP1-DT, 267 more genes
    nsv3917059copy number variation1nstd102humanPathogenic GRCh37 chr17: 45,835-12,247,218 , NCBI36 chr17: 11,807-12,187,943 , GRCh38 chr17: 162,016-12,343,901 PSMB6, RNU6-1065P, 409 more genes
    nsv3916209copy number variation1nstd102humanLikely pathogenic NCBI36 chr17: 3,894,345-5,787,816 , GRCh37 chr17: 3,947,596-5,847,092 , GRCh38 chr17: 4,044,302-5,943,772 ALOX15, ARRB2, 75 more genes
    nsv3915884copy number variation1nstd102humanPathogenic GRCh37 chr17: 45,835-6,862,369 , GRCh38 chr17: 162,088-6,959,050 , NCBI36 chr17: 11,879-6,803,093 LOC105371592, CAMKK1, 222 more genes
    nsv3915354copy number variation1nstd102humanPathogenic GRCh38 chr17: 150,732-14,764,202 , NCBI36 chr17: 525-14,608,244 , GRCh37 chr17: 525-14,667,519 KIF1C-AS1, TMEM107, 433 more genes
    nsv3913795copy number variation1nstd102humanPathogenic NCBI36 chr17: 43,098-5,496,266 , GRCh37 chr17: 45,835-5,555,542 , GRCh38 chr17: 193,307-5,652,222 BHLHA9, MNT, 194 more genes
    nsv3913013copy number variation1nstd102humanPathogenic GRCh38 chr17: 162,016-7,697,012 , GRCh37 chr17: 45,835-7,600,330 , NCBI36 chr17: 11,807-7,541,055 RPS4XP17, SNORA67, 289 more genes
    nsv3912809copy number variation1nstd102humanLikely pathogenic NCBI36 chr17: 4,759,591-5,041,145 , GRCh37 chr17: 4,818,814-5,100,421 , GRCh38 chr17: 4,915,519-5,197,126 ENO3, GP1BA, 20 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center