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 952

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144388insertion1nstd232human GRCh37.p13 chr1: 171,906,008-171,906,008 , GRCh38.p12 chr1: 171,936,868-171,936,868 DNM3
    nsv7142366insertion1nstd232human GRCh37.p13 chr1: 171,952,538-171,952,538 , GRCh38.p12 chr1: 171,983,398-171,983,398 DNM3
    nsv7099247copy number variation1nstd231human GRCh38.p12 chr1: 171,697,692-172,567,791 , GRCh37 chr1: 171,666,832-172,536,931 PIGC, VAMP4, 16 more genes
    nsv7056252inversion1nstd229human GRCh38 chr1: 172,249,192-172,249,293 , GRCh37.p13 chr1: 172,218,332-172,218,433 DNM3
    nsv7053364inversion1nstd229human GRCh38 chr1: 171,824,971-171,839,808 , GRCh37.p13 chr1: 171,794,111-171,808,948 DNM3, RPLP1P3
    nsv7051976inversion1nstd229human GRCh38 chr1: 172,357,095-172,357,114 , GRCh37.p13 chr1: 172,326,235-172,326,254 DNM3
    nsv7049570inversion1nstd229human GRCh38 chr1: 171,927,123-171,933,869 , GRCh37.p13 chr1: 171,896,263-171,903,009 DNM3
    nsv7048549inversion1nstd229human GRCh38 chr1: 172,408,579-172,408,618 , GRCh37.p13 chr1: 172,377,719-172,377,758 DNM3, LOC102724528
    nsv7043069inversion1nstd229human GRCh38 chr1: 172,366,106-172,496,936 , GRCh37.p13 chr1: 172,335,246-172,466,076 C1orf105, PIGC, 3 more genes
    nsv7042897inversion1nstd229human GRCh38 chr1: 171,883,136-171,889,399 , GRCh37.p13 chr1: 171,852,276-171,858,539 DNM3
    nsv7040287inversion1nstd229human GRCh38 chr1: 171,940,672-171,940,721 , GRCh37.p13 chr1: 171,909,812-171,909,861 DNM3
    nsv6644832copy number variation1nstd229human GRCh38 chr1: 172,342,310-172,362,971 , GRCh37.p13 chr1: 172,311,450-172,332,111 DNM3
    nsv6644831copy number variation1nstd229human GRCh38 chr1: 172,334,684-172,338,454 , GRCh37.p13 chr1: 172,303,824-172,307,594 DNM3
    nsv6644784copy number variation1nstd229human GRCh38 chr1: 172,302,685-172,308,086 , GRCh37.p13 chr1: 172,271,825-172,277,226 DNM3
    nsv6644783copy number variation1nstd229human GRCh38 chr1: 172,260,364-172,270,535 , GRCh37.p13 chr1: 172,229,504-172,239,675 DNM3
    nsv6644781copy number variation1nstd229human GRCh38 chr1: 172,212,312-172,224,069 , GRCh37.p13 chr1: 172,181,452-172,193,209 DNM3
    nsv6644780copy number variation1nstd229human GRCh38 chr1: 172,103,608-172,104,026 , GRCh37.p13 chr1: 172,072,748-172,073,166 DNM3
    nsv6644777copy number variation1nstd229human GRCh38 chr1: 172,042,476-172,042,669 , GRCh37.p13 chr1: 172,011,616-172,011,809 DNM3
    nsv6644776copy number variation1nstd229human GRCh38 chr1: 171,951,501-171,952,079 , GRCh37.p13 chr1: 171,920,641-171,921,219 DNM3
    nsv6644775copy number variation1nstd229human GRCh38 chr1: 171,927,101-171,935,000 , GRCh37.p13 chr1: 171,896,241-171,904,140 DNM3
    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