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 166

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147432insertion1nstd232human GRCh37.p13 chr5: 74,646,199-74,646,199 , GRCh38.p12 chr5: 75,350,374-75,350,374 HMGCR
    nsv7143720copy number variation1nstd232human GRCh37.p13 chr5: 74,655,132-74,655,218 , GRCh38.p12 chr5: 75,359,307-75,359,393 HMGCR
    nsv7139899insertion1nstd232human GRCh37.p13 chr5: 74,655,381-74,655,381 , GRCh38.p12 chr5: 75,359,556-75,359,556 HMGCR
    nsv7097159copy number variation2nstd102humanUncertain significance GRCh37 chr5: 73,980,960-75,008,762 , GRCh38.p12 chr5: 74,685,135-75,712,937 NSA2, RNU6-680P, 22 more genes
    nsv7045293inversion1nstd229human GRCh38 chr5: 73,247,847-76,069,477 , GRCh37.p13 chr5: 72,543,674-75,365,302 LOC107986423, NSA2, 48 more genes
    nsv7041510inversion1nstd229human GRCh38 chr5: 73,610,616-81,398,473 , GRCh37.p13 chr5: 72,906,441-80,694,292 LOC105379034, RBMX2P5, 134 more genes
    nsv6771539copy number variation1nstd229human GRCh38 chr5: 75,333,001-75,335,200 , GRCh37.p13 chr5: 74,628,826-74,631,025 HMGCR
    nsv6770347copy number variation1nstd229human GRCh38 chr5: 75,345,963-75,346,245 , GRCh37.p13 chr5: 74,641,788-74,642,070 HMGCR
    nsv6766358copy number variation1nstd229human GRCh38 chr5: 75,014,940-75,480,448 , GRCh37.p13 chr5: 74,310,765-74,776,273 ANKRD31, GCNT4, 4 more genes
    nsv6763769copy number variation1nstd229human GRCh38 chr5: 75,347,179-75,347,385 , GRCh37.p13 chr5: 74,643,004-74,643,210 HMGCR
    nsv6570338inversion1nstd223human GRCh38 chr5: 75,346,115-75,346,758 , GRCh37.p13 chr5: 74,641,940-74,642,583 HMGCR
    nsv6260504mobile element insertion1nstd215human GRCh38 chr5: 75,338,924-75,338,924 , GRCh37.p13 chr5: 74,634,749-74,634,749 HMGCR
    nsv6136132copy number variation1nstd213human GRCh37 chr5: 73,950,000-76,390,001 , GRCh38.p12 chr5: 74,654,175-77,094,176 CRHBP, F2R, 52 more genes
    nsv6135681copy number variation1nstd213human GRCh37 chr5: 74,540,000-76,140,001 , GRCh38.p12 chr5: 75,244,175-76,844,176 F2R, F2RL1, 29 more genes
    nsv6135436copy number variation1nstd213human GRCh37 chr5: 70,260,000-91,630,001 , GRCh38.p12 chr5: 70,964,173-92,334,184 , ARSB, 300 more genes
    nsv6135198copy number variation1nstd213human GRCh37 chr5: 70,130,000-76,140,001 , GRCh38.p12 chr5: 70,834,173-76,844,176 , BTF3, 117 more genes
    nsv5691073mobile element insertion2nstd211human GRCh38 chr5: 75,358,155-75,358,155 , GRCh37.p13 chr5: 74,653,980-74,653,980 HMGCR
    nsv5643490insertion1nstd207human GRCh38 chr5: 75,358,141-75,358,141 , GRCh37.p13 chr5: 74,653,966-74,653,966 HMGCR
    nsv5632473insertion1nstd207human GRCh38 chr5: 75,355,587-75,355,587 , GRCh37.p13 chr5: 74,651,412-74,651,412 HMGCR
    nsv5560947sequence alteration1nstd206human GRCh38 chr5: 74,581,386-75,393,871 , GRCh37.p13 chr5: 73,877,211-74,689,696 HEXB, GFM2, 18 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