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 860

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131063insertion1nstd186human GRCh37 chr17: 71,401,339-71,401,339 , GRCh38.p12 chr17: 73,405,200-73,405,200 SDK2
    nsv6125306copy number variation1nstd186human GRCh37 chr17: 71,385,484-71,385,712 , GRCh38.p12 chr17: 73,389,345-73,389,573 SDK2
    nsv6124397copy number variation1nstd186human GRCh37 chr17: 71,370,014-71,370,842 , GRCh38.p12 chr17: 73,373,875-73,374,703 SDK2
    nsv5979087insertion1nstd209human GRCh38 chr17: 73,504,193-73,504,193 , GRCh37.p13 chr17: 71,500,332-71,500,332 SDK2
    nsv5974637insertion1nstd209human GRCh38 chr17: 73,355,174-73,355,174 , GRCh37.p13 chr17: 71,351,313-71,351,313 SDK2
    nsv5973809insertion1nstd209human GRCh38 chr17: 73,509,902-73,509,902 , GRCh37.p13 chr17: 71,506,041-71,506,041 SDK2
    nsv5970018insertion1nstd209human GRCh38 chr17: 73,411,958-73,411,958 , GRCh37.p13 chr17: 71,408,097-71,408,097 SDK2
    nsv5940240copy number variation1nstd209human GRCh38 chr17: 73,408,065-73,408,230 , GRCh37.p13 chr17: 71,404,204-71,404,369 SDK2
    nsv5937945copy number variation1nstd209human GRCh38 chr17: 73,505,565-73,505,633 , GRCh37.p13 chr17: 71,501,704-71,501,772 SDK2
    nsv5934805copy number variation1nstd209human GRCh38 chr17: 73,376,612-73,376,686 , GRCh37.p13 chr17: 71,372,751-71,372,825 SDK2
    nsv5933799copy number variation1nstd209human GRCh38 chr17: 73,532,412-73,533,755 , GRCh37.p13 chr17: 71,528,551-71,529,894 SDK2
    nsv5933383copy number variation1nstd209human GRCh38 chr17: 73,389,374-73,389,938 , GRCh37.p13 chr17: 71,385,513-71,386,077 SDK2
    nsv5931050copy number variation1nstd209human GRCh38 chr17: 73,412,024-73,412,077 , GRCh37.p13 chr17: 71,408,163-71,408,216 SDK2
    nsv5930789copy number variation1nstd209human GRCh38 chr17: 73,376,989-73,377,066 , GRCh37.p13 chr17: 71,373,128-71,373,205 SDK2
    nsv5929645copy number variation1nstd209human GRCh38 chr17: 73,373,872-73,374,702 , GRCh37.p13 chr17: 71,370,011-71,370,841 SDK2
    nsv5928964copy number variation1nstd209human GRCh38 chr17: 73,429,191-73,429,818 , GRCh37.p13 chr17: 71,425,330-71,425,957 SDK2
    nsv5881572copy number variation1nstd209human GRCh38 chr17: 73,532,192-73,533,724 , GRCh37.p13 chr17: 71,528,331-71,529,863 SDK2
    nsv5712559mobile element insertion2nstd211human GRCh38 chr17: 73,513,072-73,513,072 , GRCh37.p13 chr17: 71,509,211-71,509,211 LOC101928251, SDK2
    nsv5701677mobile element insertion1nstd211human GRCh38 chr17: 73,502,192-73,502,192 , GRCh37.p13 chr17: 71,498,331-71,498,331 SDK2
    nsv5696605mobile element insertion1nstd211human GRCh38 chr17: 73,405,510-73,405,510 , GRCh37.p13 chr17: 71,401,649-71,401,649 SDK2
    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