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 96

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053224inversion1nstd229human GRCh38 chr6: 52,383,867-53,956,565 , GRCh37.p13 chr6: 52,248,665-53,821,363 RPA3P2, RN7SKP256, 43 more genes
    nsv7039225inversion1nstd229human GRCh38 chr6: 52,383,865-53,974,829 , GRCh37.p13 chr6: 52,248,663-53,839,627 MIR5685, GSTA8P, 43 more genes
    nsv6638066copy number variation1nstd102humanUncertain significance GRCh38 chr6: 53,151,508-58,400,428 , GRCh37.p13 chr6: 53,016,306-58,726,706 NPM1P36, LINC00680-GUSBP4, 73 more genes
    nsv6563073inversion1nstd223human GRCh38 chr6: 52,107,269-56,893,586 , GRCh37.p13 chr6: 51,972,067-56,758,384 GSTA1, LOC730101, 79 more genes
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv6007691copy number variation1nstd212human GRCh38 chr6: 53,195,165-53,195,218 , GRCh37.p13 chr6: 53,059,963-53,060,016 GCM1, SOD1P1
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5469352copy number variation1nstd206human GRCh38 chr6: 53,196,898-53,202,097 , GRCh37.p13 chr6: 53,061,696-53,066,895 GCM1, SOD1P1
    nsv5456565copy number variation1nstd206human GRCh38 chr6: 53,194,789-53,194,863 , GRCh37.p13 chr6: 53,059,587-53,059,661 GCM1, SOD1P1
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4729393copy number variation1nstd102humanUncertain significance GRCh37 chr6: 52,657,712-53,622,715 , GRCh38.p12 chr6: 52,792,914-53,757,917 KILH, GSTA6P, 29 more genes
    nsv4729270copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 48,626,041-55,575,545 , GRCh38.p12 chr6: 48,658,305-55,710,747 CRISP1, SLC25A20P1, 105 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 HLA-DPB2, CIMIP3, 1001 more genes
    nsv4143448copy number variation1nstd166human GRCh37.p13 chr6: 53,060,058-53,060,302 , GRCh38.p12 chr6: 53,195,260-53,195,504 SOD1P1, GCM1
    nsv3962814copy number variation1nstd168human GRCh38 chr6: 53,167,091-53,207,633 , GRCh37.p13 chr6: 53,031,889-53,072,431 GCM1, SOD1P1
    nsv3923721copy number variation1nstd102humanPathogenic GRCh38 chr6: 45,681,671-54,212,044 , GRCh37 chr6: 45,649,408-54,076,842 , NCBI36 chr6: 45,757,386-54,184,801 PAQR8, GSTA6P, 131 more genes
    nsv3922315copy number variation1nstd102humanPathogenic GRCh37 chr6: 50,938,895-57,297,586 , NCBI36 chr6: 51,046,854-57,405,545 , GRCh38 chr6: 50,971,182-57,432,788 MLIP-AS1, GSTA9P, 100 more genes
    nsv3910455copy number variation1nstd102humanPathogenic GRCh37 chr6: 51,061,467-53,724,432 , GRCh38 chr6: 51,093,754-53,859,634 , NCBI36 chr6: 51,169,426-53,832,391 LOC101927082, FBXO9, 58 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