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 487

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6122757copy number variation1nstd186human GRCh37 chr13: 113,325,119-113,326,317 , GRCh38.p12 chr13: 112,670,805-112,672,003 ATP11AUN
    nsv5974947insertion1nstd209human GRCh38 chr13: 112,645,365-112,645,365 , GRCh37.p13 chr13: 113,299,679-113,299,679 ATP11AUN
    nsv5971744insertion1nstd209human GRCh38 chr13: 112,678,490-112,678,490 , GRCh37.p13 chr13: 113,332,804-113,332,804 ATP11AUN
    nsv5943477copy number variation1nstd209human GRCh38 chr13: 112,670,805-112,672,002 , GRCh37.p13 chr13: 113,325,119-113,326,316 ATP11AUN
    nsv5938023copy number variation1nstd209human GRCh38 chr13: 112,673,898-112,684,837 , GRCh37.p13 chr13: 113,328,212-113,339,151 LOC102725228, ATP11AUN
    nsv5929034copy number variation1nstd209human GRCh38 chr13: 112,657,463-112,657,666 , GRCh37.p13 chr13: 113,311,777-113,311,980 ATP11AUN
    nsv5866620copy number variation1nstd209human GRCh38 chr13: 112,673,866-112,678,220 , GRCh37.p13 chr13: 113,328,180-113,332,534 ATP11AUN
    nsv5862886copy number variation1nstd209human GRCh38 chr13: 112,670,806-112,672,005 , GRCh37.p13 chr13: 113,325,120-113,326,319 ATP11AUN
    nsv5860062copy number variation1nstd209human GRCh38 chr13: 112,673,966-112,676,115 , GRCh37.p13 chr13: 113,328,280-113,330,429 ATP11AUN
    nsv5853819copy number variation1nstd209human GRCh38 chr13: 112,681,623-112,684,928 , GRCh37.p13 chr13: 113,335,937-113,339,242 LOC102725228, ATP11AUN
    nsv5848933copy number variation1nstd209human GRCh38 chr13: 112,676,926-112,684,828 , GRCh37.p13 chr13: 113,331,240-113,339,142 ATP11AUN, LOC102725228
    nsv5715358mobile element insertion1nstd211human GRCh38 chr13: 112,651,492-112,651,492 , GRCh37.p13 chr13: 113,305,806-113,305,806 ATP11AUN
    nsv5660490insertion1nstd207human GRCh38 chr13: 112,657,611-112,657,611 , GRCh37.p13 chr13: 113,311,925-113,311,925 ATP11AUN
    nsv5657209insertion1nstd207human GRCh38 chr13: 112,645,365-112,645,365 , GRCh37.p13 chr13: 113,299,679-113,299,679 ATP11AUN
    nsv5653734insertion1nstd207human GRCh38 chr13: 112,657,713-112,657,713 , GRCh37.p13 chr13: 113,312,027-113,312,027 ATP11AUN
    nsv5652826insertion1nstd207human GRCh38 chr13: 112,666,297-112,666,297 , GRCh37.p13 chr13: 113,320,611-113,320,611 ATP11AUN
    nsv5651028insertion1nstd207human GRCh38 chr13: 112,678,490-112,678,490 , GRCh37.p13 chr13: 113,332,804-113,332,804 ATP11AUN
    nsv5650834insertion1nstd207human GRCh38 chr13: 112,657,754-112,657,754 , GRCh37.p13 chr13: 113,312,068-113,312,068 ATP11AUN
    nsv5594095copy number variation1nstd207human GRCh38 chr13: 112,657,543-112,657,695 , GRCh37.p13 chr13: 113,311,857-113,312,009 ATP11AUN
    nsv5593958copy number variation1nstd207human GRCh38 chr13: 112,657,696-112,657,746 , GRCh37.p13 chr13: 113,312,010-113,312,060 ATP11AUN
    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