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 99

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097529copy number variation1nstd102humanUncertain significance GRCh37 chr5: 32,355,866-32,786,451 , GRCh38.p12 chr5: 32,355,760-32,786,345 TMEM183AP2, NPR3, 4 more genes
    nsv7048370inversion1nstd229human GRCh38 chr5: 31,943,969-32,642,096 , GRCh37.p13 chr5: 31,944,075-32,642,202 RPL27P10, GOLPH3, 10 more genes
    nsv7039407inversion1nstd229human GRCh38 chr5: 32,373,124-34,861,255 , GRCh37.p13 chr5: 32,373,230-34,861,360 TTC23L, LOC105374715, 31 more genes
    nsv7038918inversion1nstd229human GRCh38 chr5: 31,932,933-32,628,546 , GRCh37.p13 chr5: 31,933,039-32,628,652 RNU6-378P, RPL27P10, 10 more genes
    nsv6770174copy number variation1nstd229human GRCh38 chr5: 32,170,252-32,417,269 , GRCh37.p13 chr5: 32,170,358-32,417,374 GOLPH3, RNU6-1079P, 5 more genes
    nsv6762717copy number variation1nstd229human GRCh38 chr5: 32,195,713-32,417,756 , GRCh37.p13 chr5: 32,195,819-32,417,861 MTMR12, MIR579, 4 more genes
    nsv6636973copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,348,753-46,389,339 , GRCh38.p12 chr5: 29,348,646-46,389,237 SUB1, LOC105374740, 210 more genes
    nsv6562950inversion1nstd223human GRCh38 chr5: 32,392,821-32,393,413 , GRCh37.p13 chr5: 32,392,927-32,393,519 ZFR, MIR579
    nsv6557004inversion1nstd223human GRCh38 chr5: 31,943,968-32,642,088 , GRCh37.p13 chr5: 31,944,074-32,642,194 LINC02061, SUB1, 10 more genes
    nsv6394517copy number variation1nstd223human GRCh38 chr5: 32,195,713-32,417,750 , GRCh37.p13 chr5: 32,195,819-32,417,855 RNU6-1079P, ZFR, 4 more genes
    nsv6313864copy number variation1nstd102humanPathogenic GRCh37 chr5: 26,382,110-46,389,339 , GRCh38.p12 chr5: 26,382,001-46,389,237 LOC107986346, RNU6-760P, 227 more genes
    nsv6300383copy number variation1nstd186human GRCh37 chr5: 26,834,087-43,674,516 , GRCh38.p12 chr5: 26,833,978-43,674,414 , TMEM267, 221 more genes
    nsv6135406copy number variation1nstd213human GRCh37 chr5: 31,280,000-36,080,001 , GRCh38.p12 chr5: 31,279,893-36,079,899 IL7R, NPR3, 64 more genes
    nsv6135175copy number variation1nstd213human GRCh37 chr5: 29,210,000-46,400,001 , GRCh38.p12 chr5: 29,209,893-46,399,899 CDH6, HMGCS1, 210 more genes
    nsv5471384copy number variation1nstd206human GRCh38 chr5: 26,833,978-43,674,414 , GRCh37.p13 chr5: 26,834,087-43,674,516 , INTS6P1, 221 more genes
    nsv5381781copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,081,195-45,294,031 , GRCh38.p12 chr5: 29,081,088-45,293,929 ST3GAL5P1, LOC105374711, 213 more genes
    nsv4762598inversion1nstd199human GRCh37 chr5: 20,832,595-34,371,602 , GRCh38.p12 chr5: 20,832,486-34,371,497 , CDH6, 117 more genes
    nsv4751404inversion1nstd199human GRCh37 chr5: 20,834,824-34,371,606 , GRCh38.p12 chr5: 20,834,715-34,371,501 , CDH6, 117 more genes
    nsv4674644copy number variation1nstd102humanUncertain significance GRCh37 chr5: 29,720,391-34,124,081 , GRCh38.p12 chr5: 29,720,284-34,123,976 C1QTNF3, LOC105374703, 54 more genes
    nsv4548939insertion1nstd166human GRCh37.p13 chr5: 32,392,594-32,392,594 , GRCh38.p12 chr5: 32,392,488-32,392,488 MIR579, ZFR
    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