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 324

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076785inversion1nstd229human GRCh38 chr20: 36,001,722-37,069,571 , GRCh37.p13 chr20: 34,589,644-35,697,974 RPS3AP3, EPB41L1-AS1, 22 more genes
    nsv7028662copy number variation1nstd229human GRCh38 chr20: 36,746,479-36,832,051 , GRCh37.p13 chr20: 35,374,882-35,460,454 NDRG3, DSN1, 1 more genes
    nsv7027677copy number variation1nstd229human GRCh38 chr20: 36,838,899-36,838,954 , GRCh37.p13 chr20: 35,467,302-35,467,357 MTCL2
    nsv7023995copy number variation1nstd229human GRCh38 chr20: 36,849,634-36,852,715 , GRCh37.p13 chr20: 35,478,037-35,481,118 MTCL2
    nsv7023734copy number variation1nstd229human GRCh38 chr20: 36,810,977-36,811,012 , GRCh37.p13 chr20: 35,439,380-35,439,415 MTCL2
    nsv7021466copy number variation1nstd229human GRCh38 chr20: 36,859,235-36,861,817 , GRCh37.p13 chr20: 35,487,638-35,490,220 MTCL2
    nsv7021198copy number variation1nstd229human GRCh38 chr20: 33,145,032-41,995,765 , GRCh37.p13 chr20: 31,732,838-40,624,405 PXMP4, RPL12P11, 199 more genes
    nsv7020829copy number variation1nstd229human GRCh38 chr20: 36,807,796-36,829,899 , GRCh37.p13 chr20: 35,436,199-35,458,302 MTCL2
    nsv7020177copy number variation1nstd229human GRCh38 chr20: 36,801,699-36,878,314 , GRCh37.p13 chr20: 35,430,102-35,506,717 MTCL2, TLDC2, 1 more genes
    nsv7020060copy number variation1nstd229human GRCh38 chr20: 36,859,936-36,860,150 , GRCh37.p13 chr20: 35,488,339-35,488,553 MTCL2
    nsv7018629copy number variation1nstd229human GRCh38 chr20: 36,683,202-36,775,933 , GRCh37.p13 chr20: 35,311,605-35,404,336 DSN1, MTCL2, 1 more genes
    nsv7018604copy number variation1nstd229human GRCh38 chr20: 36,783,357-36,815,256 , GRCh37.p13 chr20: 35,411,760-35,443,659 MTCL2
    nsv6637546copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 29,652,122-35,603,726 , GRCh38.p12 chr20: 30,417,446-36,975,323 AHCY, ASIP, 195 more genes
    nsv6533774copy number variation1nstd223human GRCh38 chr20: 36,852,998-36,913,501 , GRCh37.p13 chr20: 35,481,401-35,541,904 MTCL2, TLDC2, 2 more genes
    nsv6523163copy number variation1nstd223human GRCh38 chr20: 36,847,745-36,852,777 , GRCh37.p13 chr20: 35,476,148-35,481,180 MTCL2
    nsv6517725copy number variation1nstd223human GRCh38 chr20: 36,859,235-36,861,808 , GRCh37.p13 chr20: 35,487,638-35,490,211 MTCL2
    nsv6291474copy number variation1nstd102humanUncertain significance GRCh37 chr20: 35,335,325-35,606,892 , GRCh38.p12 chr20: 36,706,922-36,978,489 TLDC2, SAMHD1, 4 more genes
    nsv6277735copy number variation1nstd214human GRCh38 chr20: 36,858,267-36,858,418 , GRCh37.p13 chr20: 35,486,670-35,486,821 MTCL2
    nsv6251414mobile element insertion1nstd215human GRCh38 chr20: 36,809,051-36,809,051 , GRCh37.p13 chr20: 35,437,454-35,437,454 MTCL2
    nsv6211424copy number variation1nstd214human GRCh38 chr20: 36,858,391-36,858,478 , GRCh37.p13 chr20: 35,486,794-35,486,881 MTCL2
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Find related data

    Recent activity

    Support Center