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 403

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7096119copy number variation2nstd102humanUncertain significance GRCh37 chr2: 189,839,216-192,012,929 , GRCh38.p12 chr2: 188,974,490-191,148,203 NAB1, ANKAR, 38 more genes
    nsv7054842inversion1nstd229human GRCh38 chr2: 190,054,200-190,773,498 , GRCh37.p13 chr2: 190,918,926-191,638,224 NAB1, NEMP2-DT, 7 more genes
    nsv7049643inversion1nstd229human GRCh38 chr2: 190,231,387-190,234,284 , GRCh37.p13 chr2: 191,096,113-191,099,010 HIBCH
    nsv7046391inversion1nstd229human GRCh38 chr2: 190,291,330-190,291,366 , GRCh37.p13 chr2: 191,156,056-191,156,092 HIBCH
    nsv6697760copy number variation1nstd229human GRCh38 chr2: 190,296,914-190,302,913 , GRCh37.p13 chr2: 191,161,640-191,167,639 HIBCH
    nsv6697587copy number variation1nstd229human GRCh38 chr2: 190,313,804-190,322,506 , GRCh37.p13 chr2: 191,178,530-191,187,232 HIBCH
    nsv6696442copy number variation1nstd229human GRCh38 chr2: 190,303,401-190,310,400 , GRCh37.p13 chr2: 191,168,127-191,175,126 HIBCH
    nsv6694547copy number variation1nstd229human GRCh38 chr2: 190,152,692-190,244,172 , GRCh37.p13 chr2: 191,017,418-191,108,898 HIBCH, C2orf88
    nsv6688198copy number variation1nstd229human GRCh38 chr2: 190,247,592-190,249,869 , GRCh37.p13 chr2: 191,112,318-191,114,595 HIBCH
    nsv6685780copy number variation1nstd229human GRCh38 chr2: 190,276,545-190,276,618 , GRCh37.p13 chr2: 191,141,271-191,141,344 HIBCH
    nsv6683812copy number variation1nstd229human GRCh38 chr2: 190,199,802-190,209,348 , GRCh37.p13 chr2: 191,064,528-191,074,074 C2orf88, HIBCH
    nsv6683026copy number variation1nstd229human GRCh38 chr2: 190,308,823-190,313,321 , GRCh37.p13 chr2: 191,173,549-191,178,047 HIBCH
    nsv6680592copy number variation1nstd229human GRCh38 chr2: 190,309,091-190,318,362 , GRCh37.p13 chr2: 191,173,817-191,183,088 HIBCH
    nsv6679938copy number variation1nstd229human GRCh38 chr2: 190,241,285-190,241,706 , GRCh37.p13 chr2: 191,106,011-191,106,432 HIBCH
    nsv6679233copy number variation1nstd229human GRCh38 chr2: 190,276,701-190,280,600 , GRCh37.p13 chr2: 191,141,427-191,145,326 HIBCH
    nsv6678961copy number variation1nstd229human GRCh38 chr2: 190,269,927-190,275,150 , GRCh37.p13 chr2: 191,134,653-191,139,876 HIBCH
    nsv6637127copy number variation1nstd102humanPathogenic GRCh37 chr2: 189,909,904-209,468,383 , GRCh38.p12 chr2: 189,045,178-208,603,658 LOC100421409, LOC100507443, 310 more genes
    nsv6636571copy number variation1nstd102humanPathogenic GRCh37 chr2: 187,152,754-199,960,525 , GRCh38.p12 chr2: 186,288,027-199,095,802 GAPDHP59, OSGEPL1-AS1, 135 more genes
    nsv6636257copy number variation1nstd102humanUncertain significance GRCh37 chr2: 190,819,533-191,102,271 , GRCh38.p12 chr2: 189,954,807-190,237,545 C2orf88, MSTN, 1 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