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 94

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5688225mobile element insertion2nstd211human GRCh38 chr6: 29,460,815-29,460,815 , GRCh37.p13 chr6: 29,428,592-29,428,592 OR2H1
    nsv5402666mobile element insertion1nstd206human GRCh38 chr6: 29,460,815-29,460,866 , GRCh37.p13 chr6: 29,428,592-29,428,643 OR2H1
    nsv5119539mobile element insertion1nstd203human GRCh38 chr6: 29,456,187-29,456,211 , GRCh37.p13 chr6: 29,423,964-29,423,988 OR2H1, OR5V1, 1 more genes
    nsv5105757mobile element insertion1nstd203human GRCh38 chr6: 29,460,800-29,460,815 , GRCh37.p13 chr6: 29,428,577-29,428,592 OR2H1
    nsv5036471inversion1nstd200human GRCh38 chr6: 25,888,426-29,704,316 , GRCh37.p13 chr6: 25,888,654-29,672,093 , OR11A1, 368 more genes
    nsv4879678inversion1nstd200human GRCh37 chr6: 25,888,654-29,672,093 , GRCh38.p12 chr6: 25,888,426-29,704,316 , H1-4, 368 more genes
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv3921510copy number variation1nstd102humanUncertain significance NCBI36 chr6: 29,407,237-29,556,283 , GRCh37.p13 chr6: 29,299,258-29,448,304 , GRCh38.p12 chr6: 29,331,481-29,480,527 OR5V1, OR11A1, 10 more genes
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
    nsv3912336copy number variation1nstd102humanUncertain significance GRCh37 chr6: 28,730,964-29,737,605 , GRCh38 chr6: 28,763,187-29,769,828 , NCBI36 chr6: 28,838,943-29,845,584 OR2AD1P, UBD, 87 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
    nsv3888352copy number variation1nstd102humanUncertain significance GRCh37 chr6: 28,735,761-29,585,573 , GRCh38.p12 chr6: 28,767,984-29,617,796 OR12D1, LOC105379641, 75 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
    nsv3870570copy number variation1nstd102humanUncertain significance GRCh37 chr6: 28,130,359-32,108,367 , GRCh38.p12 chr6: 28,162,581-32,140,590 LOC105375002, SKIC2, 345 more genes
    nsv3169066inversion1nstd158human GRCh37 chr6: 5,923,377-99,717,885 , GRCh38.p12 chr6: 5,923,144-99,270,009 , ABCF1, 1877 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Find related data

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    Support Center