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 216

    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
    nsv7148124copy number variation1nstd102humanPathogenic GRCh37 chr8: 118,185,471-126,635,744 , GRCh38.p12 chr8: 117,173,232-125,623,500 LINC02964, TATDN1, 115 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
    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
    nsv6838222copy number variation1nstd229human GRCh38 chr8: 125,385,401-125,431,100 , GRCh37.p13 chr8: 126,397,643-126,443,342 TRIB1
    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
    nsv6136309copy number variation1nstd213human GRCh37 chr8: 122,920,000-127,650,001 , GRCh38.p12 chr8: 121,907,761-126,637,756 TBC1D31, FAM91A1, 77 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
    nsv6135822copy number variation1nstd213human GRCh37 chr8: 124,520,000-127,320,001 , GRCh38.p12 chr8: 123,507,760-126,307,756 RNF139, LINC00964, 42 more genes
    nsv5481671copy number variation1nstd206human GRCh38 chr8: 125,271,778-125,569,813 , GRCh37.p13 chr8: 126,284,020-126,582,057 LINC02964, TRIB1, 1 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4679444copy number variation1nstd189human GRCh37.p13 chr8: 125,927,352-126,453,448 , GRCh38.p12 chr8: 124,915,110-125,441,206 SQLE, WASHC5, 8 more genes
    nsv4675718copy number variation1nstd102humanUncertain significance GRCh37 chr8: 124,878,368-126,737,708 , GRCh38.p12 chr8: 123,866,128-125,725,464 FER1L6-AS1, SQLE-DT, 30 more genes
    nsv4675273copy number variation1nstd102humanPathogenic GRCh37 chr8: 121,042,467-146,295,771 , GRCh38.p12 chr8: 120,030,228-145,070,385 TOP1MT, SLA, 379 more genes
    nsv4480077mobile element insertion1nstd166human GRCh37.p13 chr8: 126,447,397-126,447,397 , GRCh38.p12 chr8: 125,435,155-125,435,155 TRIB1
    nsv4457220copy number variation1nstd102humanPathogenic GRCh37 chr8: 123,074,293-131,113,892 , GRCh38.p12 chr8: 122,062,054-130,101,646 ZHX1-C8orf76, SMILR, 117 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