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 140

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096308copy number variation1nstd102humanUncertain significance GRCh37 chr22: 35,776,672-42,486,826 , GRCh38.p12 chr22: 35,380,679-42,090,822 CDC42EP1, SREBF2, 231 more genes
    nsv7095836copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr22: 37,154,355-39,148,633 , GRCh38.p12 chr22: 36,758,311-38,752,628 CSF2RBP1, H1-0, 80 more genes
    nsv7078067inversion1nstd229human GRCh38 chr22: 30,287,061-38,012,264 , GRCh37.p13 chr22: 30,683,050-38,408,271 LINC02885, RN7SL20P, 203 more genes
    nsv7072766inversion1nstd229human GRCh38 chr22: 35,603,617-39,341,195 , GRCh37.p13 chr22: 35,999,664-39,737,200 APOL5, MTATP6P20, 132 more genes
    nsv7072171inversion1nstd229human GRCh38 chr22: 34,919,966-36,817,658 , GRCh37.p13 chr22: 35,315,956-37,213,702 APOL4, RBFOX2, 45 more genes
    nsv7065768inversion1nstd229human GRCh38 chr22: 36,745,255-36,817,941 , GRCh37.p13 chr22: 37,141,299-37,213,985 PVALB, CACNG2-DT, 1 more genes
    nsv7065500inversion1nstd229human GRCh38 chr22: 29,260,563-37,652,385 , GRCh37.p13 chr22: 29,656,552-38,048,392 RFPL1, PATZ1, 217 more genes
    nsv7064066inversion1nstd229human GRCh38 chr22: 34,920,312-39,418,308 , GRCh37.p13 chr22: 35,316,302-39,814,313 LOC112268295, APOBEC3B-AS1, 150 more genes
    nsv7059210inversion1nstd229human GRCh38 chr22: 35,603,611-39,337,136 , GRCh37.p13 chr22: 35,999,658-39,733,141 MTCO2P20, RPS29P31, 132 more genes
    nsv7026588copy number variation1nstd229human GRCh38 chr22: 36,570,594-37,316,473 , GRCh37.p13 chr22: 36,966,641-37,712,514 LL22NC01-81G9.3, IFT27, 24 more genes
    nsv7024970copy number variation1nstd229human GRCh38 chr22: 36,756,884-36,756,958 , GRCh37.p13 chr22: 37,152,928-37,153,002 CACNG2-DT, IFT27
    nsv7024654copy number variation1nstd229human GRCh38 chr22: 36,352,908-37,059,696 , GRCh37.p13 chr22: 36,748,953-37,455,736 NCF4-AS1, TST, 23 more genes
    nsv7023516copy number variation1nstd229human GRCh38 chr22: 36,764,778-36,767,840 , GRCh37.p13 chr22: 37,160,822-37,163,884 CACNG2-DT, IFT27
    nsv7019987copy number variation1nstd229human GRCh38 chr22: 36,672,990-36,911,370 , GRCh37.p13 chr22: 37,069,036-37,307,412 NCF4, NCF4-AS1, 5 more genes
    nsv6555486copy number variation1nstd223human GRCh38 chr22: 36,768,851-36,769,599 , GRCh37.p13 chr22: 37,164,895-37,165,643 IFT27
    nsv6224137copy number variation1nstd214human GRCh38 chr22: 36,756,880-36,756,952 , GRCh37.p13 chr22: 37,152,924-37,152,996 CACNG2-DT, IFT27
    nsv6134212copy number variation1nstd213human GRCh37 chr22: 36,430,000-39,960,001 , GRCh38.p12 chr22: 36,033,952-39,563,996 ATF4, COX5BP7, 133 more genes
    nsv5965049copy number variation1nstd209human GRCh38 chr22: 36,756,880-36,756,952 , GRCh37.p13 chr22: 37,152,924-37,152,996 CACNG2-DT, IFT27
    nsv5536764copy number variation1nstd206human GRCh38 chr22: 36,756,884-36,756,953 , GRCh37.p13 chr22: 37,152,928-37,152,997 CACNG2-DT, IFT27
    nsv5360552translocation1nstd200human GRCh38 chr22: 36,756,953-36,756,953 , GRCh38 chr22: 36,756,884-36,756,884 , GRCh37.p13 chr22: 37,152,997-37,152,997 , GRCh37.p13 chr22: 37,152,928-37,152,928 CACNG2-DT, IFT27
    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