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 211

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148238copy number variation1nstd102humanPathogenic GRCh38 chr8: 115,586,904-135,607,135 , GRCh37.p13 chr8: 116,599,131-136,619,378 CCDC26, EFR3A, 238 more genes
    nsv7077533inversion1nstd229human GRCh38 chr8: 125,245,829-133,039,076 , GRCh37.p13 chr8: 126,258,071-134,051,321 PVT1, MTRF1LP2, 76 more genes
    nsv7065808inversion1nstd229human GRCh38 chr8: 127,938,115-127,947,706 , GRCh37.p13 chr8: 128,950,361-128,959,952 LINC02912, PVT1
    nsv7062540inversion1nstd229human GRCh38 chr8: 126,857,766-129,574,185 , GRCh37.p13 chr8: 127,870,011-130,586,431 CASC21, POU5F1B, 28 more genes
    nsv6857318copy number variation1nstd229human GRCh38 chr8: 126,364,525-132,576,581 , GRCh37.p13 chr8: 127,376,770-133,588,829 PRNCR1, MIR1205, 59 more genes
    nsv6857205copy number variation1nstd229human GRCh38 chr8: 127,935,701-127,947,700 , GRCh37.p13 chr8: 128,947,947-128,959,946 LINC02912, PVT1
    nsv6856000copy number variation1nstd229human GRCh38 chr8: 124,373,188-128,390,224 , GRCh37.p13 chr8: 125,385,429-129,402,470 WASHC5, MIR4662B, 57 more genes
    nsv6851226copy number variation1nstd229human GRCh38 chr8: 127,936,201-127,947,700 , GRCh37.p13 chr8: 128,948,447-128,959,946 PVT1, LINC02912
    nsv6637224copy number variation1nstd102humanPathogenic GRCh37 chr8: 112,234,557-133,668,379 , GRCh38.p12 chr8: 111,222,328-132,656,133 RNU4-37P, LOC100420215, 220 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6314744copy number variation1nstd102humanPathogenic GRCh37 chr8: 96,496,503-146,295,711 , GRCh38.p12 chr8: 95,484,275-145,070,325 OSR2, LOC392268, 676 more genes
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6290242copy number variation1nstd102humanUncertain significance GRCh37 chr8: 128,878,931-141,662,233 , GRCh38.p12 chr8: 127,866,685-140,652,134 LINC02055, LOC101927798, 100 more genes
    nsv6137048copy number variation1nstd213human GRCh37 chr8: 128,200,000-131,040,001 , GRCh38.p12 chr8: 127,187,755-130,027,755 CYRIB, GSDMC, 29 more genes
    nsv6136318copy number variation1nstd213human GRCh37 chr8: 128,550,000-134,990,001 , GRCh38.p12 chr8: 127,537,755-133,977,758 CCN4, PHF20L1, 67 more genes
    nsv6136082copy number variation1nstd213human GRCh37 chr8: 86,730,000-142,740,001 , GRCh38.p12 chr8: 85,717,771-141,729,803 ANXA13, ATP6V1C1, 658 more genes
    nsv6135827copy number variation1nstd213human GRCh37 chr8: 128,610,000-129,230,001 , GRCh38.p12 chr8: 127,597,755-128,217,755 MYC, MIR1206, 10 more genes
    nsv6135826copy number variation1nstd213human GRCh37 chr8: 127,420,000-129,170,001 , GRCh38.p12 chr8: 126,407,755-128,157,755 SRRM1P1, MIR1206, 26 more genes
    nsv5976748inversion1nstd209human GRCh38 chr8: 127,947,710-127,957,305 , GRCh37.p13 chr8: 128,959,956-128,969,551 PVT1, LINC02912
    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