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 148

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098791copy number variation1nstd102humanPathogenic GRCh37 chr17: 55,442,363-56,309,063 , GRCh38.p12 chr17: 57,365,002-58,231,702 MKS1, OR4D2, 21 more genes
    nsv7098766copy number variation1nstd102humanPathogenic GRCh37 chr17: 55,806,534-56,540,597 , GRCh38.p12 chr17: 57,729,173-58,463,236 SRSF1, LOC105371840, 24 more genes
    nsv6988034copy number variation1nstd229human GRCh38 chr17: 57,983,239-58,340,473 , GRCh37.p13 chr17: 56,060,600-56,417,834 MIR4736, LOC105371841, 16 more genes
    nsv6634423copy number variation1nstd102humanPathogenic GRCh37 chr17: 55,043,662-56,728,123 , GRCh38.p12 chr17: 56,966,301-58,650,762 RNU7-134P, DYNLL2-DT, 42 more genes
    nsv6310393copy number variation1nstd102humanUncertain significance GRCh37 chr17: 54,671,585-59,938,900 , GRCh38.p12 chr17: 56,594,224-61,861,539 RNF43, LOC107985048, 132 more genes
    nsv6133316copy number variation1nstd213human GRCh37 chr17: 53,930,000-62,410,001 , GRCh38.p12 chr17: 55,852,639-64,332,641 CA4, CD79B, 208 more genes
    nsv5933652copy number variation1nstd209human GRCh38 chr17: 58,087,220-58,089,138 , GRCh37.p13 chr17: 56,164,581-56,166,499 DYNLL2
    nsv5930052copy number variation1nstd209human GRCh38 chr17: 58,083,681-58,087,078 , GRCh37.p13 chr17: 56,161,042-56,164,439 DYNLL2, DYNLL2-DT
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5530947copy number variation1nstd206human GRCh38 chr17: 58,087,223-58,089,139 , GRCh37.p13 chr17: 56,164,584-56,166,500 DYNLL2
    nsv5530211copy number variation1nstd206human GRCh38 chr17: 58,092,343-58,092,453 , GRCh37.p13 chr17: 56,169,704-56,169,814 DYNLL2
    nsv5515455copy number variation1nstd206human GRCh38 chr17: 58,083,683-58,087,079 , GRCh37.p13 chr17: 56,161,044-56,164,440 DYNLL2-DT, DYNLL2
    nsv5358993translocation1nstd200human GRCh38 chr17: 58,089,139-58,089,139 , GRCh38 chr17: 58,087,223-58,087,223 , GRCh37.p13 chr17: 56,164,584-56,164,584 , GRCh37.p13 chr17: 56,166,500-56,166,500 DYNLL2
    nsv5335413translocation1nstd200human GRCh37 chr17: 56,164,584-56,164,584 , GRCh37 chr17: 56,166,500-56,166,500 , GRCh38.p12 chr17: 58,087,223-58,087,223 , GRCh38.p12 chr17: 58,089,139-58,089,139 DYNLL2
    nsv4624483copy number variation1nstd183human GRCh37 chr17: 56,168,150-56,168,735 , GRCh38.p12 chr17: 58,090,789-58,091,374 DYNLL2
    nsv4573591mobile element insertion1nstd166human GRCh37.p13 chr17: 56,169,222-56,169,222 , GRCh38.p12 chr17: 58,091,861-58,091,861 DYNLL2
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4261681copy number variation1nstd166human GRCh37.p13 chr17: 56,158,334-56,158,876 , GRCh38.p12 chr17: 58,080,973-58,081,515 DYNLL2, DYNLL2-DT
    nsv3920623copy number variation1nstd102humanPathogenic GRCh37 chr17: 54,760,866-56,162,300 , NCBI36 chr17: 52,115,865-53,517,299 , GRCh38 chr17: 56,683,505-58,084,939 C17orf67, CUEDC1, 28 more genes
    nsv3917224copy number variation1nstd102humanPathogenic GRCh38 chr17: 56,958,745-58,171,125 , NCBI36 chr17: 52,391,105-53,603,485 , GRCh37 chr17: 55,036,106-56,248,486 MRPS23, MSX2P1, 24 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