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 516

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148242copy number variation1nstd102humanPathogenic GRCh38 chr15: 20,966,971-25,963,714 , GRCh37.p13 chr15: 21,172,300-26,208,861 LOC101269108, LOC107983983, 227 more genes
    nsv7148111copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,742,396-28,567,325 , GRCh38.p12 chr15: 23,319,714-28,322,179 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 SNORD116-18, PWAR4, 246 more genes
    nsv7148097copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,605,427-28,566,579 , GRCh38.p12 chr15: 23,360,280-28,321,433 LOC107984770, SNORD115-31, 147 more genes
    nsv7137213copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-30,386,398 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-30,094,195 TVP23BP1, SNORD115-1, 247 more genes
    nsv7137100copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,684,691-28,566,579 , GRCh38.p12 chr15: 23,439,544-28,321,433 DMAC1P1, SNORD116-16, 142 more genes
    nsv7098883copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,406,271-28,566,579 , GRCh38.p12 chr15: 23,319,714-28,321,433 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 LOC105370739, SNORD116-27, 246 more genes
    nsv7093407copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,833,525-28,544,662 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,299,516 UBE2CP4, SERPINE4P, 246 more genes
    nsv7093400copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,684,645-28,566,612 , GRCh38.p12 chr15: 23,439,498-28,321,466 SNORD115-45, SNORD107, 142 more genes
    nsv7067542inversion1nstd229human GRCh38 chr15: 23,549,781-28,456,830 , GRCh37.p13 chr15: 23,794,928-28,701,976 SNORD115-34, LOC107984787, 148 more genes
    nsv7065496inversion1nstd229human GRCh38 chr15: 20,672,644-28,900,286 , GRCh37.p13 chr15: 20,877,973-29,145,432 SNURF, LOC101060118, 290 more genes
    nsv7062202inversion1nstd229human GRCh38 chr15: 24,015,385-25,754,615 , GRCh37.p13 chr15: 24,260,532-25,999,762 ATP10A, SNORD115-4, 107 more genes
    nsv7060175inversion1nstd229human GRCh38 chr15: 23,786,777-25,729,649 , GRCh37.p13 chr15: 24,031,924-25,974,796 SNORD115-26, LOC107984787, 107 more genes
    nsv6973165copy number variation1nstd229human GRCh38 chr15: 23,199,056-28,429,484 , GRCh37.p13 chr15: 23,564,855-28,674,630 LOC102723564, SNORD115-2, 162 more genes
    nsv6969131copy number variation1nstd229human GRCh38 chr15: 22,744,959-28,819,371 , GRCh37.p13 chr15: 23,564,855-29,064,517 RNA5SP391, PDCD6IPP1, 195 more genes
    nsv6637778copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,422-28,545,601 , GRCh38.p12 chr15: 23,319,714-28,300,455 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 LOC107984779, ULK4P1, 246 more genes
    nsv6637596copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,290,787-28,560,269 , GRCh38.p12 chr15: 23,319,714-28,315,123 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 SNORD115-23, DEPDC1P1, 246 more genes
    nsv6637553copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,422-30,386,553 , GRCh38.p12 chr15: 23,319,714-30,094,350 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 FAN1, LOC105370751, 247 more genes
    nsv6637498copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,670,891-28,561,671 , GRCh38.p12 chr15: 23,425,744-28,316,525 LOC107984770, SNORD115-34, 143 more genes
    nsv6637482copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,620,192-28,545,459 , GRCh38.p12 chr15: 23,375,045-28,300,313 PWRN1, SNORD116-28, 143 more genes
    nsv6637399copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,422-28,545,355 , GRCh38.p12 chr15: 23,319,714-28,300,209 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 DNM1P28, MIR4508, 246 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