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 97

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5665187inversion1nstd207human GRCh38 chr6: 71,641,254-71,652,655 , GRCh37.p13 chr6: 72,350,957-72,362,358 RNU4-66P
    nsv5033711inversion1nstd200human GRCh38 chr6: 66,790,667-77,039,639 , GRCh37.p13 chr6: 67,500,560-77,749,356 , FAM135A-AS1, 116 more genes
    nsv4729236copy number variation1nstd102humanUncertain significance GRCh37 chr6: 71,351,541-72,837,211 , GRCh38.p12 chr6: 70,641,838-72,127,508 LOC105377850, LOC105377853, 17 more genes
    nsv4675762copy number variation1nstd102humanUncertain significance GRCh37 chr6: 72,181,114-72,765,924 , GRCh38.p12 chr6: 71,471,411-72,056,221 RIMS1, NGRNP2, 3 more genes
    nsv4604820copy number variation1nstd183human GRCh37 chr6: 64,732,117-73,192,183 , GRCh38.p12 chr6: 64,022,224-72,482,481 LOC105377847, LOC105377850, 64 more genes
    nsv4455775copy number variation1nstd102humanPathogenic GRCh37 chr6: 69,481,460-73,185,349 , GRCh38.p12 chr6: 68,771,568-72,475,647 KRT19P1, BECN1P2, 34 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv3924180copy number variation1nstd102humanPathogenic NCBI36 chr6: 65,316,269-84,193,229 , GRCh38 chr6: 64,549,655-83,426,791 , GRCh37 chr6: 65,259,548-84,136,510 LOC105377875, KCNQ5-IT1, 188 more genes
    nsv3920009copy number variation1nstd102humanUncertain significance NCBI36 chr6: 71,575,615-72,708,133 , GRCh38 chr6: 70,809,191-71,941,709 , GRCh37 chr6: 71,518,894-72,651,412 SMAP1, MIR30C2, 15 more genes
    nsv3916496copy number variation1nstd102humanUncertain significance GRCh38 chr6: 70,794,142-71,972,780 , GRCh37 chr6: 71,503,845-72,682,483 , NCBI36 chr6: 71,560,566-72,739,204 KRT19P1, BECN1P2, 15 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
    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
    esv4011098complex chromosomal rearrangement4estd236human GRCh37 chr6: 48,385,249-154,434,404 , GRCh38.p12 chr6: 48,417,513-154,113,269 , ACTBP8, 1274 more genes
    nsv3169066inversion1nstd158human GRCh37 chr6: 5,923,377-99,717,885 , GRCh38.p12 chr6: 5,923,144-99,270,009 , ABCF1, 1877 more genes
    nsv3168939inversion1nstd158human GRCh37 chr6: 12,268,690-80,058,596 , GRCh38.p12 chr6: 12,268,457-79,348,879 , ABCF1, 1548 more genes
    nsv3168805inversion1nstd158human GRCh37 chr6: 12,296,990-80,059,394 , GRCh38.p12 chr6: 12,296,757-79,349,677 , ABCF1, 1548 more genes
    nsv3168551inversion1nstd158human GRCh37 chr6: 7,798,260-81,124,626 , GRCh38.p12 chr6: 7,798,027-80,414,909 , ABCF1, 1644 more genes
    nsv3168209copy number variation1nstd158human GRCh38.p12 chr6: 56,099,235-128,190,528 , GRCh37 chr6: 55,964,033-128,511,673 , ACTBP8, 798 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