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 144

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112738copy number variation1nstd102humanPathogenic GRCh37 chr6: 149,619-3,951,208 , GRCh38.p12 chr6: 149,619-3,950,974 LINC01600, TUBB2BP1, 66 more genes
    nsv5457724copy number variation1nstd206human GRCh38 chr6: 3,234,390-3,234,548 , GRCh37.p13 chr6: 3,234,624-3,234,782 LOC100422781
    nsv4729315copy number variation1nstd102humanPathogenic GRCh37 chr6: 302,183-3,290,583 , GRCh38.p12 chr6: 302,183-3,290,349 RIPK1, MARK2P18, 53 more genes
    nsv4675919copy number variation1nstd102humanUncertain significance GRCh37 chr6: 3,175,377-3,233,433 , GRCh38.p12 chr6: 3,175,143-3,233,199 LINC02525, TUBB2B, 2 more genes
    nsv4675760copy number variation1nstd102humanUncertain significance GRCh37 chr6: 3,157,162-3,233,433 , GRCh38.p12 chr6: 3,156,928-3,233,199 TUBB2A, TUBB2BP1, 4 more genes
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4371355copy number variation1nstd173human GRCh37 chr6: 3,157,163-3,233,433 , GRCh38.p12 chr6: 3,156,929-3,233,199 TUBB2A, TUBB2B, 4 more genes
    nsv4369920copy number variation1nstd173human GRCh37 chr6: 3,157,163-3,232,759 , GRCh38.p12 chr6: 3,156,929-3,232,525 TUBB2B, LINC02525, 4 more genes
    nsv4118676copy number variation1nstd166human GRCh37.p13 chr6: 3,234,624-3,234,782 , GRCh38.p12 chr6: 3,234,390-3,234,548 LOC100422781
    nsv3955250insertion1nstd168human GRCh38 chr6: 3,206,518-3,248,806 , GRCh37.p13 chr6: 3,206,752-3,249,040 LOC100422781, TUBB2B
    nsv3923249copy number variation1nstd102humanPathogenic NCBI36 chr6: 110,675-8,981,266 , GRCh38 chr6: 165,675-9,036,034 , GRCh37 chr6: 165,675-9,036,267 LOC100506207, LOC105374889, 148 more genes
    nsv3923206copy number variation1nstd102humanPathogenic NCBI36 chr6: 108,083-3,404,840 , GRCh38 chr6: 163,083-3,459,607 , GRCh37 chr6: 163,083-3,459,841 LOC105374883, MIR4645, 58 more genes
    nsv3922576copy number variation1nstd102humanPathogenic GRCh37 chr6: 164,633-6,284,470 , GRCh38 chr6: 164,633-6,284,237 , NCBI36 chr6: 109,633-6,229,469 GLRX3P2, CDYL, 106 more genes
    nsv3922052copy number variation1nstd102humanPathogenic GRCh37 chr6: 155,807-17,058,645 , NCBI36 chr6: 100,807-17,166,624 , GRCh38 chr6: 155,807-17,058,414 ECI2-DT, RNU1-11P, 268 more genes
    nsv3921817copy number variation1nstd102humanPathogenic GRCh37 chr6: 2,862,874-16,698,019 , GRCh38 chr6: 2,862,640-16,697,788 , NCBI36 chr6: 2,807,873-16,805,998 RN7SKP293, LOC105374906, 230 more genes
    nsv3921201copy number variation1nstd102humanUncertain significance NCBI36 chr6: 101,974-4,892,090 , GRCh37 chr6: 156,974-4,947,091 , GRCh38 chr6: 156,974-4,946,857 LOC100422781, RN7SL352P, 86 more genes
    nsv3921027copy number variation1nstd102humanPathogenic GRCh38 chr6: 389,423-13,474,956 , GRCh37 chr6: 389,423-13,475,188 , NCBI36 chr6: 334,423-13,583,167 LOC105374898, HIVEP1, 215 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
    nsv3920236copy number variation1nstd102humanPathogenic GRCh37 chr6: 164,633-5,823,834 , GRCh38 chr6: 164,633-5,823,601 , NCBI36 chr6: 109,633-5,768,833 TUBB2A, SERPINB9-AS1, 98 more genes
    nsv3918645copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 101,974-11,659,036 , GRCh37 chr6: 156,974-11,551,050 , GRCh38 chr6: 156,974-11,550,817 BMP6, BPHL, 194 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