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 124

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099232copy number variation1nstd231human GRCh38.p12 chr1: 151,364,317-152,231,192 , GRCh37 chr1: 151,336,793-152,203,668 , PSMB4, 37 more genes
    nsv7095245copy number variation1nstd102humanUncertain significance GRCh37 chr1: 151,801,885-152,287,932 , GRCh38.p12 chr1: 151,829,409-152,315,456 S100A10, C2CD4D, 18 more genes
    nsv7056666inversion1nstd229human GRCh38 chr1: 151,403,323-155,722,147 , GRCh37.p13 chr1: 151,375,799-155,691,938 ILF2, SPRR2C, 219 more genes
    nsv7056211inversion1nstd229human GRCh38 chr1: 143,881,700-152,159,818 , GRCh37.p13 chr1|NW_003871055.3: 697,113-7,283,150 , PDIA3P1, 333 more genes
    nsv7044458inversion1nstd229human GRCh38 chr1: 150,355,899-155,246,175 , GRCh37.p13 chr1: 150,440,214-155,215,966 LCE2C, MUC1, 254 more genes
    nsv7042502inversion1nstd229human GRCh38 chr1: 150,301,267-155,517,761 , GRCh37.p13 chr1: 150,440,214-155,487,552 LINGO4, CELF3, 268 more genes
    nsv6642183copy number variation1nstd229human GRCh38 chr1: 152,072,606-152,090,677 , GRCh37.p13 chr1: 152,045,082-152,063,153 SPTLC1P4, LOC100131107, 1 more genes
    nsv6642035copy number variation1nstd229human GRCh38 chr1: 152,030,507-152,250,018 , GRCh37.p13 chr1: 152,002,983-152,222,494 S100A11, TCHHL1, 7 more genes
    nsv6310678copy number variation4nstd102humanUncertain significance GRCh37 chr1: 149,895,434-156,851,434 , GRCh38.p12 chr1: 149,923,542-156,881,642 PRPF3, KHDC4, 352 more genes
    nsv6133734copy number variation1nstd213human GRCh37 chr1: 150,350,000-154,440,001 , GRCh38.p12 chr1: 150,377,524-154,467,525 , MCL1, 216 more genes
    nsv6133732copy number variation1nstd213human GRCh37 chr1: 149,750,000-153,310,001 , GRCh38.p12 chr1: 149,778,444-153,337,525 , CTSK, 183 more genes
    nsv6133556copy number variation1nstd213human GRCh37 chr1: 151,990,000-152,390,001 , GRCh38.p12 chr1: 152,017,524-152,417,525 , LOC100131107, 15 more genes
    nsv6133500copy number variation1nstd213human GRCh37 chr1: 151,850,000-152,430,001 , GRCh38.p12 chr1: 151,877,524-152,457,525 , S100A10, 18 more genes
    nsv6133499copy number variation1nstd213human GRCh37 chr1: 149,880,000-153,720,001 , GRCh38.p12 chr1: 149,908,448-153,747,525 , CTSK, 198 more genes
    nsv6048887insertion1nstd212human GRCh38 chr1: 152,082,756-152,082,756 , GRCh37.p13 chr1: 152,055,232-152,055,232 TCHHL1
    nsv5955734insertion1nstd209human GRCh38 chr1: 152,082,756-152,082,756 , GRCh37.p13 chr1: 152,055,232-152,055,232 TCHHL1
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4711935copy number variation1nstd195human GRCh37 chr1: 151,624,751-152,167,951 , GRCh38.p12 chr1: 151,652,275-152,195,475 , S100A11, 28 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