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 126

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7042065inversion1nstd229human GRCh38 chr6: 88,046,652-88,046,826 , GRCh37.p13 chr6: 88,756,370-88,756,544 SPACA1
    nsv7039342inversion1nstd229human GRCh38 chr6: 86,041,090-92,871,248 , GRCh37.p13 chr6: 86,750,808-93,580,966 NDUFA5P9, AKIRIN2, 85 more genes
    nsv6808037copy number variation1nstd229human GRCh38 chr6: 88,033,871-88,130,359 , GRCh37.p13 chr6: 88,743,589-88,840,078 SPACA1
    nsv6634392copy number variation1nstd102humanUncertain significance GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297 MTHFD2P2, RPL7P27, 212 more genes
    nsv6410410copy number variation1nstd223human GRCh38 chr6: 88,033,871-88,130,355 , GRCh37.p13 chr6: 88,743,589-88,840,074 SPACA1
    nsv6313857copy number variation1nstd102humanPathogenic GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492 LOC101928570, RNU4-72P, 288 more genes
    nsv6135938copy number variation1nstd213human GRCh37 chr6: 87,590,000-89,360,001 , GRCh38.p12 chr6: 86,880,282-88,650,282 ACTBP8, CGA, 33 more genes
    nsv6135855copy number variation1nstd213human GRCh37 chr6: 87,530,000-91,880,001 , GRCh38.p12 chr6: 86,820,282-91,170,283 ACTBP8, CGA, 67 more genes
    nsv6135527copy number variation1nstd213human GRCh37 chr6: 87,520,000-91,880,001 , GRCh38.p12 chr6: 86,810,282-91,170,283 ACTBP8, CGA, 67 more genes
    nsv5111550mobile element insertion1nstd203human GRCh38 chr6: 88,065,501-88,065,512 , GRCh37.p13 chr6: 88,775,219-88,775,230 SPACA1
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4945393copy number variation1nstd200human GRCh38 chr6: 88,050,987-88,076,397 , GRCh37.p13 chr6: 88,760,705-88,786,115 SPACA1
    nsv4942030copy number variation1nstd200human GRCh38 chr6: 88,048,553-88,050,358 , GRCh37.p13 chr6: 88,758,271-88,760,076 SPACA1
    nsv4824533copy number variation1nstd200human GRCh37 chr6: 88,760,705-88,786,115 , GRCh38.p12 chr6: 88,050,987-88,076,397 SPACA1
    nsv4816924copy number variation1nstd200human GRCh37 chr6: 88,758,271-88,760,076 , GRCh38.p12 chr6: 88,048,553-88,050,358 SPACA1
    nsv4675337copy number variation1nstd102humanUncertain significance GRCh37 chr6: 88,412,786-89,246,061 , GRCh38.p12 chr6: 87,703,068-88,536,342 LOC101928936, LOC105377882, 9 more genes
    nsv4675039copy number variation1nstd102humanPathogenic GRCh37 chr6: 86,024,761-90,023,713 , GRCh38.p12 chr6: 85,315,043-89,313,994 C6orf163, LOC100652960, 65 more genes
    nsv4562634mobile element insertion1nstd166human GRCh37.p13 chr6: 88,770,744-88,770,744 , GRCh38.p12 chr6: 88,061,026-88,061,026 SPACA1
    nsv4524197copy number variation1nstd166human GRCh37.p13 chr6: 88,775,242-88,775,480 , GRCh38.p12 chr6: 88,065,524-88,065,762 SPACA1
    nsv4484188mobile element insertion1nstd166human GRCh37.p13 chr6: 88,773,726-88,773,726 , GRCh38.p12 chr6: 88,064,008-88,064,008 SPACA1
    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