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 142

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4965528copy number variation1nstd200human GRCh38 chr8: 80,979,415-81,477,850 , GRCh37.p13 chr8: 81,891,650-82,390,085 LOC105375925, PMP2, 8 more genes
    nsv4729032copy number variation1nstd102humanUncertain significance GRCh37 chr8: 81,895,303-82,546,283 , GRCh38.p12 chr8: 80,983,068-81,634,048 PMP2, NIPA2P4, 14 more genes
    nsv4457069copy number variation1nstd102humanUncertain significance GRCh37 chr8: 82,276,728-82,641,699 , GRCh38.p12 chr8: 81,364,493-81,729,464 PMP2, IMPA1, 11 more genes
    nsv4456862copy number variation1nstd102humanUncertain significance GRCh37 chr8: 82,307,170-82,408,647 , GRCh38.p12 chr8: 81,394,935-81,496,412 FABP9, LOC101927118, 2 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4456123copy number variation1nstd102humanUncertain significance GRCh37 chr8: 82,196,649-85,352,499 , GRCh38.p12 chr8: 81,284,414-84,440,264 CHMP4C, LINC02839, 30 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4332062inversion1nstd166human GRCh37.p13 chr8: 70,438,609-99,073,700 , GRCh38.p12 chr8: 69,526,374-98,061,472 , FTH1P11, 375 more genes
    nsv4318515inversion1nstd166human GRCh37.p13 chr8: 75,861,320-132,789,960 , GRCh38.p12 chr8: 74,949,085-131,777,713 , ANXA13, 716 more genes
    nsv3923698copy number variation1nstd102humanPathogenic NCBI36 chr8: 79,617,219-84,706,949 , GRCh37.p13 chr8: 79,454,664-84,544,394 , GRCh38.p12 chr8: 78,542,429-83,632,159 RPS26P34, PAG1, 77 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3923011copy number variation1nstd102humanPathogenic GRCh38 chr8: 66,171,669-93,505,509 , GRCh37 chr8: 67,083,904-94,517,737 , NCBI36 chr8: 67,246,458-94,586,913 CA3, HAUS1P3, 353 more genes
    nsv3922848copy number variation1nstd102humanPathogenic NCBI36 chr8: 74,954,174-86,710,947 , GRCh37 chr8: 74,791,620-86,523,695 , GRCh38 chr8: 73,879,385-85,611,466 MITA1, CA3-AS1, 139 more genes
    nsv3922631copy number variation1nstd102humanPathogenic GRCh38 chr8: 61,691,800-82,537,696 , NCBI36 chr8: 62,766,913-83,612,486 , GRCh37 chr8: 62,604,359-83,449,931 NCOA2, LOC107986893, 284 more genes
    nsv3919841copy number variation1nstd102humanPathogenic GRCh38 chr8: 78,614,077-145,054,634 , GRCh37 chr8: 79,526,312-146,280,020 , NCBI36 chr8: 79,688,867-146,250,824 LY6S-AS1, LOC107984017, 911 more genes
    nsv3919282copy number variation1nstd102humanPathogenic GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824 MIR4662B, LOC101927845, 2104 more genes
    nsv3919200copy number variation1nstd102humanPathogenic GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639 LOC112268023, LOC105375925, 2103 more genes
    nsv3918908copy number variation1nstd102humanLikely benign GRCh37 chr8: 82,100,916-82,956,065 , GRCh38 chr8: 81,188,681-82,043,830 , NCBI36 chr8: 82,263,471-83,118,620 LOC105375925, FABP4, 18 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