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 457

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148187copy number variation1nstd102humanPathogenic GRCh38 chr1: 224,304,638-224,434,886 , GRCh37.p13 chr1: 224,492,340-224,622,588 NVL, CNIH4, 4 more genes
    nsv7146171copy number variation1nstd232human GRCh37.p13 chr1: 224,505,495-224,505,578 , GRCh38.p12 chr1: 224,317,793-224,317,876 NVL
    nsv7144883insertion1nstd232human GRCh37.p13 chr1: 224,477,437-224,477,437 , GRCh38.p12 chr1: 224,289,735-224,289,735 NVL
    nsv7099264copy number variation1nstd231human GRCh38.p12 chr1: 222,151,895-226,849,338 , GRCh37 chr1: 222,325,237-227,037,039 PARP1, CAPN2, 99 more genes
    nsv7093371copy number variation1nstd102humannot provided GRCh37 chr1: 224,230,307-243,181,599 , GRCh38.p12 chr1: 224,042,605-243,018,297 RPL36P6, MTND4LP21, 377 more genes
    nsv6675709copy number variation1nstd229human GRCh38 chr1: 224,161,301-224,385,400 , GRCh37.p13 chr1: 224,349,003-224,573,102 LOC101927164, FBXO28, 8 more genes
    nsv6674651copy number variation1nstd229human GRCh38 chr1: 224,228,569-224,237,164 , GRCh37.p13 chr1: 224,416,271-224,424,866 NVL
    nsv6673899copy number variation1nstd229human GRCh38 chr1: 224,265,446-224,267,604 , GRCh37.p13 chr1: 224,453,148-224,455,306 NVL
    nsv6673745copy number variation1nstd229human GRCh38 chr1: 224,162,401-224,287,000 , GRCh37.p13 chr1: 224,350,103-224,474,702 LOC724084, LOC101927143, 5 more genes
    nsv6673622copy number variation1nstd229human GRCh38 chr1: 224,329,357-224,332,014 , GRCh37.p13 chr1: 224,517,059-224,519,716 NVL
    nsv6673056copy number variation1nstd229human GRCh38 chr1: 224,295,301-224,307,100 , GRCh37.p13 chr1: 224,483,003-224,494,802 NVL, RNU6-1008P
    nsv6669118copy number variation1nstd229human GRCh38 chr1: 224,241,019-224,247,712 , GRCh37.p13 chr1: 224,428,721-224,435,414 NVL
    nsv6668350copy number variation1nstd229human GRCh38 chr1: 224,252,864-224,257,877 , GRCh37.p13 chr1: 224,440,566-224,445,579 MIR320B2, NVL
    nsv6667535copy number variation1nstd229human GRCh38 chr1: 224,271,751-224,272,598 , GRCh37.p13 chr1: 224,459,453-224,460,300 NVL
    nsv6662132copy number variation1nstd229human GRCh38 chr1: 224,168,559-224,280,818 , GRCh37.p13 chr1: 224,356,261-224,468,520 DEGS1, LOC724084, 4 more genes
    nsv6638068copy number variation1nstd102humanassociation GRCh38 chr1: 208,430,918-228,938,006 , GRCh37.p13 chr1: 208,604,263-229,073,753 AURKAP1, TLR5, 372 more genes
    nsv6636794copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,972,939-249,224,684 , GRCh38.p12 chr1: 223,785,237-248,930,485 SEPTIN7P13, WNT3A, 546 more genes
    nsv6636736copy number variation1nstd102humanUncertain significance GRCh37 chr1: 221,325,488-225,804,228 , GRCh38.p12 chr1: 221,152,146-225,616,526 BROX, LINC02765, 77 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6555203inversion1nstd223human GRCh38 chr1: 224,295,224-224,295,683 , GRCh37.p13 chr1: 224,482,926-224,483,385 NVL
    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