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 178

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5537855insertion1nstd206human GRCh38 chr6: 99,421,496-99,421,503 , GRCh37.p13 chr6: 99,869,372-99,869,379 PNISR
    nsv5369519translocation1nstd200human GRCh38 chr6: 99,408,951-99,408,951 , GRCh38 chr6: 99,409,063-99,409,063 , GRCh37.p13 chr6: 99,856,827-99,856,827 , GRCh37.p13 chr6: 99,856,939-99,856,939 PNISR
    nsv5118148mobile element insertion1nstd203human GRCh38 chr6: 99,419,152-99,419,190 , GRCh37.p13 chr6: 99,867,028-99,867,066 PNISR
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4945467copy number variation1nstd200human GRCh38 chr6: 99,417,643-99,419,049 , GRCh37.p13 chr6: 99,865,519-99,866,925 PNISR
    nsv4942451copy number variation1nstd200human GRCh38 chr6: 99,396,955-99,397,087 , GRCh37.p13 chr6: 99,844,831-99,844,963 PNISR
    nsv4817213copy number variation1nstd200human GRCh37 chr6: 99,850,087-99,850,208 , GRCh38.p12 chr6: 99,402,211-99,402,332 PNISR
    nsv4768376copy number variation1nstd102humanPathogenic GRCh37 chr6: 98,949,950-114,533,905 , GRCh38.p12 chr6: 98,502,074-114,212,741 LOC101927405, GPR6, 211 more genes
    nsv4675136copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 98,870,687-100,270,433 , GRCh38.p12 chr6: 98,422,811-99,822,557 CCNC, POU3F2, 13 more genes
    nsv4544819insertion1nstd166human GRCh37.p13 chr6: 99,869,372-99,869,372 , GRCh38.p12 chr6: 99,421,496-99,421,496 PNISR
    nsv4457050copy number variation1nstd102humanUncertain significance GRCh37 chr6: 99,158,119-100,269,911 , GRCh38.p12 chr6: 98,710,243-99,822,035 TSTD3, BDH2P1, 12 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv4312499inversion1nstd166human GRCh37.p13 chr6: 94,532,001-117,422,619 , GRCh38.p12 chr6: 93,822,283-117,101,456 , CRYBG1, 284 more genes
    nsv4141490copy number variation1nstd166human GRCh37.p13 chr6: 99,844,831-99,844,963 , GRCh38.p12 chr6: 99,396,955-99,397,087 PNISR
    nsv3924576copy number variation1nstd102humanPathogenic NCBI36 chr6: 97,164,591-122,524,393 , GRCh38 chr6: 96,609,994-122,161,548 , GRCh37 chr6: 97,057,870-122,482,694 TUBE1, PLN, 318 more genes
    nsv3921775copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 97,691,375-103,286,627 , GRCh37.p13 chr6: 97,584,654-103,179,934 , GRCh38.p12 chr6: 97,136,778-102,732,059 CCNC, GRIK2, 38 more genes
    nsv3921137copy number variation1nstd102humanPathogenic GRCh37 chr6: 99,116,405-101,714,826 , GRCh38 chr6: 98,668,529-101,266,950 , NCBI36 chr6: 99,223,126-101,821,547 MIR548AI, BDH2P1, 25 more genes
    nsv3920677copy number variation1nstd102humanUncertain significance NCBI36 chr6: 98,965,717-100,385,804 , GRCh37.p13 chr6: 98,858,996-100,279,083 , GRCh38.p12 chr6: 98,411,120-99,831,207 PNISR-AS1, PNKY, 13 more genes
    nsv3919111copy number variation1nstd102humanPathogenic GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637 RNU6-770P, MAP3K5-AS2, 810 more genes
    nsv3917149copy number variation1nstd102humanUncertain significance GRCh37 chr6: 99,218,523-100,260,987 , GRCh38 chr6: 98,770,647-99,813,111 , NCBI36 chr6: 99,325,244-100,367,708 PNKY, PNISR-AS1, 12 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