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 152

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7043423inversion1nstd229human GRCh38 chr6: 49,733,069-49,733,118 , GRCh37.p13 chr6: 49,700,782-49,700,831 CRISP3
    nsv6797587copy number variation1nstd229human GRCh38 chr6: 49,737,993-49,738,124 , GRCh37.p13 chr6: 49,705,706-49,705,837 CRISP3
    nsv6795271copy number variation1nstd229human GRCh38 chr6: 49,332,174-50,024,818 , GRCh37.p13 chr6: 49,299,844-49,992,531 DEFB114, LOC101927020, 16 more genes
    nsv6791174copy number variation1nstd229human GRCh38 chr6: 49,494,055-50,046,260 , GRCh37.p13 chr6: 49,461,768-50,013,973 DEFB110, CRISP1, 13 more genes
    nsv6789968copy number variation1nstd229human GRCh38 chr6: 49,738,400-49,857,157 , GRCh37.p13 chr6: 49,706,113-49,824,870 LOC101927020, CRISP1, 3 more genes
    nsv6789367copy number variation1nstd229human GRCh38 chr6: 48,645,525-49,878,656 , GRCh37.p13 chr6: 48,613,261-49,846,369 LOC100421158, CYP2AC1P, 14 more genes
    nsv6785085copy number variation1nstd229human GRCh38 chr6: 49,671,798-49,741,903 , GRCh37.p13 chr6: 49,639,511-49,709,616 CRISP2, CRISP3
    nsv6782047copy number variation1nstd229human GRCh38 chr6: 49,731,514-49,731,677 , GRCh37.p13 chr6: 49,699,227-49,699,390 CRISP3
    nsv6780716copy number variation1nstd229human GRCh38 chr6: 49,736,932-49,741,995 , GRCh37.p13 chr6: 49,704,645-49,709,708 CRISP3
    nsv6404787copy number variation1nstd223human GRCh38 chr6: 49,736,960-49,737,547 , GRCh37.p13 chr6: 49,704,673-49,705,260 CRISP3
    nsv6404392copy number variation1nstd223human GRCh38 chr6: 49,743,567-49,744,077 , GRCh37.p13 chr6: 49,711,280-49,711,790 CRISP3
    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
    nsv6290935copy number variation1nstd102humanUncertain significance GRCh37 chr6: 49,459,881-50,012,992 , GRCh38.p12 chr6: 49,492,168-50,045,279 DEFB133, PGK2, 14 more genes
    nsv6136508copy number variation1nstd213human GRCh37 chr6: 49,700,000-50,020,001 , GRCh38.p12 chr6: 49,732,287-50,052,288 DEFB113, LOC101927020, 8 more genes
    nsv6136507copy number variation1nstd213human GRCh37 chr6: 49,420,000-49,700,001 , GRCh38.p12 chr6: 49,452,287-49,732,288 MMUT, RHAG, 6 more genes
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5473625copy number variation1nstd206human GRCh38 chr6: 49,690,434-49,880,145 , GRCh37.p13 chr6: 49,658,147-49,847,858 CRISP1, PGK2, 4 more genes
    nsv5040265inversion1nstd200human GRCh38 chr6: 49,481,877-49,812,356 , GRCh37.p13 chr6: 49,449,590-49,780,069 PGK2, RHAG, 7 more genes
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 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