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 148

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148249copy number variation1nstd102humanPathogenic GRCh38 chr6: 113,857,248-130,442,177 , GRCh37.p13 chr6: 114,178,427-130,763,322 TRDN-AS1, LOC100420743, 179 more genes
    nsv7137202copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 112,713,854-124,105,184 , GRCh38.p12 chr6: 112,392,652-123,784,039 COL10A1, FABP7, 129 more genes
    nsv7093381copy number variation1nstd102humannot provided GRCh37 chr6: 119,243,634-126,078,530 , GRCh38.p12 chr6: 118,922,469-125,757,384 HEY2-AS1, SERINC1, 52 more genes
    nsv7052079inversion1nstd229human GRCh38 chr6: 119,644,000-123,115,000 , GRCh37.p13 chr6: 119,965,161-123,436,145 RNA5SP215, RNU4-35P, 28 more genes
    nsv7051442inversion1nstd229human GRCh38 chr6: 120,525,437-125,245,762 , GRCh37.p13 chr6: 120,846,583-125,566,908 RNF217-AS1, HSF2, 35 more genes
    nsv7048680inversion1nstd229human GRCh38 chr6: 120,128,256-123,693,128 , GRCh37.p13 chr6: 120,449,402-124,014,273 TRDN-AS1, TBC1D32, 30 more genes
    nsv6817028copy number variation1nstd229human GRCh38 chr6: 118,002,640-125,132,407 , GRCh37.p13 chr6: 118,323,803-125,453,553 GJA1, COX6A1P3, 56 more genes
    nsv6811905copy number variation1nstd229human GRCh38 chr6: 121,432,168-121,463,348 , GRCh37.p13 chr6: 121,753,314-121,784,494 RNU4-35P, GJA1
    nsv6801527copy number variation1nstd229human GRCh38 chr6: 121,394,501-121,597,500 , GRCh37.p13 chr6: 121,715,647-121,918,646 GJA1, RNU2-8P, 4 more genes
    nsv6636964copy number variation1nstd102humanUncertain significance GRCh37 chr6: 121,646,369-124,675,332 , GRCh38.p12 chr6: 121,325,223-124,354,186 HMGN2P29, ATP5MGP2, 27 more genes
    nsv6636864copy number variation1nstd102humanUncertain significance GRCh37 chr6: 120,059,951-130,033,233 , GRCh38.p12 chr6: 119,738,805-129,712,088 LOC107986640, ECHDC1, 93 more genes
    nsv6568941inversion1nstd223human GRCh38 chr6: 120,593,241-123,536,832 , GRCh37.p13 chr6: 120,914,387-123,857,977 RNU4-35P, SMPDL3A, 28 more genes
    nsv6566945inversion1nstd223human GRCh38 chr6: 121,450,095-121,450,304 , GRCh37.p13 chr6: 121,771,241-121,771,450 GJA1
    nsv6315321copy number variation1nstd102humanPathogenic GRCh38 chr6: 115,941,808-133,892,653 , GRCh37.p13 chr6: 116,262,971-134,213,791 SLC18B1, ARHGAP18, 223 more genes
    nsv6312550copy number variation1nstd102humanUncertain significance GRCh37 chr6: 121,401,917-121,769,142 , GRCh38.p12 chr6: 121,080,771-121,447,996 GJA1, RNU6-1286P, 3 more genes
    nsv6291288copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 117,441,803-123,349,672 , GRCh38.p12 chr6: 117,120,640-123,028,527 FABP7, GJA1, 61 more genes
    nsv6135713copy number variation1nstd213human GRCh37 chr6: 121,690,000-121,860,001 , GRCh38.p12 chr6: 121,368,854-121,538,855 GJA1, LOC260339, 3 more genes
    nsv5564276copy number variation1nstd102humanUncertain significance GRCh37 chr6: 121,767,974-121,769,162 , GRCh38.p12 chr6: 121,446,828-121,448,016 GJA1
    nsv5369694translocation1nstd200human GRCh38 chr6: 121,441,351-121,441,351 , GRCh38 chr6: 121,441,558-121,441,558 , GRCh37.p13 chr6: 121,762,497-121,762,497 , GRCh37.p13 chr6: 121,762,704-121,762,704 GJA1
    nsv5107736mobile element insertion1nstd203human GRCh38 chr6: 121,436,872-121,436,881 , GRCh37.p13 chr6: 121,758,018-121,758,027 GJA1
    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