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 90

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5100274mobile element insertion1nstd203human GRCh38 chr6: 87,396,279-87,396,291 , GRCh37.p13 chr6: 88,105,997-88,106,009 LINC01590
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4942006copy number variation1nstd200human GRCh38 chr6: 87,388,558-87,424,457 , GRCh37.p13 chr6: 88,098,276-88,134,175 TAF13P1, LINC01590, 1 more genes
    nsv4675039copy number variation1nstd102humanPathogenic GRCh37 chr6: 86,024,761-90,023,713 , GRCh38.p12 chr6: 85,315,043-89,313,994 C6orf163, LOC100652960, 65 more genes
    nsv4457169copy number variation1nstd102humanUncertain significance GRCh37 chr6: 88,095,499-88,341,035 , GRCh38.p12 chr6: 87,385,781-87,631,317 ST13P16, CFAP206, 7 more genes
    nsv4456405copy number variation1nstd102humanUncertain significance GRCh37 chr6: 87,627,836-93,698,486 , GRCh38.p12 chr6: 86,918,118-92,988,768 MIR4643, LOC107986625, 82 more genes
    nsv3961096insertion1nstd168human GRCh38 chr6: 87,399,633-87,420,741 , GRCh37.p13 chr6: 88,109,351-88,130,459 LINC01590, CFAP206
    nsv3923528copy number variation1nstd102humanPathogenic NCBI36 chr6: 84,604,741-99,376,910 , GRCh38 chr6: 83,838,303-98,822,313 , GRCh37 chr6: 84,548,022-99,270,189 RNU4-72P, LOC100132830, 157 more genes
    nsv3922883copy number variation1nstd102humanPathogenic NCBI36 chr6: 85,811,199-89,199,075 , GRCh37.p13 chr6: 85,754,480-89,142,356 , GRCh38.p12 chr6: 85,044,762-88,432,637 RN7SL643P, RPL7P27, 57 more genes
    nsv3921478copy number variation1nstd102humanPathogenic NCBI36 chr6: 76,692,636-93,477,232 , GRCh38 chr6: 75,926,199-92,710,793 , GRCh37 chr6: 76,635,916-93,420,511 SPACA1, TAF13P1, 187 more genes
    nsv3919111copy number variation1nstd102humanPathogenic GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637 RNU6-770P, MAP3K5-AS2, 810 more genes
    nsv3918084copy number variation1nstd102humanPathogenic GRCh37 chr6: 86,513,991-93,898,976 , GRCh38 chr6: 85,804,273-93,189,258 , NCBI36 chr6: 86,570,710-93,955,697 LOC105377897, GABRR2, 91 more genes
    nsv3915571copy number variation1nstd102humanUncertain significance GRCh38 chr6: 87,050,381-87,535,518 , NCBI36 chr6: 87,816,818-88,301,955 , GRCh37 chr6: 87,760,099-88,245,236 C6orf163, RARS2, 16 more genes
    nsv3914309copy number variation1nstd102humanPathogenic GRCh38 chr6: 82,569,098-93,753,476 , NCBI36 chr6: 83,335,534-94,519,915 , GRCh37 chr6: 83,278,815-94,463,194 ME1, GJB7, 136 more genes
    nsv3912992copy number variation1nstd102humanPathogenic GRCh38 chr6: 85,370,716-90,669,793 , NCBI36 chr6: 86,137,153-91,436,233 , GRCh37 chr6: 86,080,434-91,379,512 DNAJC19P6, RNU4-12P, 88 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3880626copy number variation1nstd102humanPathogenic GRCh37 chr6: 85,988,428-120,548,687 , GRCh38.p12 chr6: 85,278,710-120,227,541 LOC107986534, FYN, 426 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 RNU6-411P, LOC107986611, 2910 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 LOC105378061, MIR4640, 2914 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