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 84

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv3920975copy number variation1nstd102humanPathogenic GRCh37 chr6: 141,454,127-169,739,666 , GRCh38 chr6: 141,132,990-169,339,571 , NCBI36 chr6: 141,495,820-169,481,591 UST-AS2, LOC729681, 394 more genes
    nsv3920651copy number variation1nstd102humanPathogenic GRCh38 chr6: 144,932,561-152,985,364 , NCBI36 chr6: 145,295,390-153,348,192 , GRCh37 chr6: 145,253,697-153,306,499 PPP1R14C, RAET1K, 107 more genes
    nsv3915150copy number variation1nstd102humanPathogenic NCBI36 chr6: 124,322,082-156,156,864 , GRCh37.p13 chr6: 124,280,383-156,115,172 , GRCh38.p12 chr6: 123,959,238-155,794,038 KATNA1, RNF217-AS1, 422 more genes
    nsv3911993copy number variation1nstd102humanPathogenic NCBI36 chr6: 133,900,102-166,209,023 , GRCh38 chr6: 133,537,271-165,875,545 , GRCh37 chr6: 133,858,409-166,289,033 LOC105369171, SHPRH, 418 more genes
    nsv3911164copy number variation1nstd102humanPathogenic NCBI36 chr6: 135,720,981-155,817,943 , GRCh37 chr6: 135,679,288-155,776,251 , GRCh38 chr6: 135,358,150-155,455,117 HYMAI, SMIM28, 263 more genes
    nsv3910985copy number variation1nstd102humanPathogenic NCBI36 chr6: 146,843,948-151,790,457 , GRCh37 chr6: 146,802,255-151,748,764 , GRCh38 chr6: 146,481,119-151,427,629 RMND1, LOC645967, 77 more genes
    nsv3904637copy number variation1nstd102humanPathogenic GRCh37 chr6: 144,947,731-150,266,155 , GRCh38.p12 chr6: 144,626,595-149,945,019 LOC107986660, CCT7P1, 59 more genes
    nsv3898363copy number variation1nstd102humanUncertain significance GRCh37 chr6: 146,652,354-148,108,890 , GRCh38.p12 chr6: 146,331,218-147,787,754 LUADT1, GRM1, 12 more genes
    nsv3891146copy number variation1nstd102humanPathogenic GRCh37 chr6: 139,513,020-150,389,231 , GRCh38.p12 chr6: 139,191,883-150,068,095 UST, RAET1K, 131 more genes
    nsv3890752copy number variation1nstd102humanPathogenic GRCh37 chr6: 144,075,695-152,337,005 , GRCh38.p12 chr6: 143,754,558-152,015,870 LOC105378052, RNU6-302P, 109 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
    nsv3168744inversion1nstd158human GRCh37 chr6: 81,126,432-158,470,478 , GRCh38.p12 chr6: 80,416,715-158,049,446 , ACTBP8, 985 more genes
    nsv3168167copy number variation1nstd158human GRCh37 chr6: 12,299,904-158,472,787 , GRCh38.p12 chr6: 12,299,671-158,051,755 , ABCF1, 2551 more genes
    nsv3168015copy number variation1nstd158human GRCh38.p12 chr6: 80,242,023-157,646,271 , GRCh37 chr6: 80,951,740-158,067,303 , ACTBP8, 979 more genes
    esv4010717copy number variation1estd233human GRCh38.p12 chr6: 135,913,862-167,283,512 , GRCh37 chr6: 136,235,000-167,697,000 , ACAT2, 439 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