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
    nsv5634757insertion1nstd207human GRCh38 chr6: 110,857,542-110,857,542 , GRCh37.p13 chr6: 111,178,745-111,178,745 CNN2P9, AMD1
    nsv5564516copy number variation1nstd102humanUncertain significance GRCh37 chr6: 109,796,301-113,083,437 , GRCh38.p12 chr6: 109,475,098-112,762,235 RN7SL617P, METTL24, 67 more genes
    nsv5239038copy number variation1nstd204human GRCh38.p13 chr6: 110,811,861-110,873,911 , GRCh37.p13 chr6: 111,133,064-111,195,114 CNN2P9, RNU6-1115P, 3 more genes
    nsv5225844copy number variation1nstd204human GRCh38.p13 chr6: 110,812,701-110,917,600 , GRCh37.p13 chr6: 111,133,904-111,238,803 AMD1, SNORA40C, 3 more genes
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4768376copy number variation1nstd102humanPathogenic GRCh37 chr6: 98,949,950-114,533,905 , GRCh38.p12 chr6: 98,502,074-114,212,741 LOC101927405, GPR6, 211 more genes
    nsv4685989copy number variation1nstd102humanPathogenic GRCh37 chr6: 101,287,058-117,013,245 , GRCh38.p12 chr6: 100,839,182-116,692,082 RPL23AP50, RNU6-960P, 216 more genes
    nsv4674911copy number variation1nstd102humanUncertain significance GRCh37 chr6: 109,564,694-112,232,351 , GRCh38.p12 chr6: 109,243,491-111,911,148 LOC105377939, LOC105377945, 57 more genes
    nsv4613071copy number variation1nstd183human GRCh37 chr6: 111,121,311-111,382,035 , GRCh38.p12 chr6: 110,800,108-111,060,832 CNN2P9, RNU6-1115P, 8 more genes
    nsv4457007copy number variation1nstd102humanPathogenic GRCh37 chr6: 110,981,075-119,608,396 , GRCh38.p12 chr6: 110,659,872-119,287,231 HDAC2-AS2, NIP7P3, 134 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv4312499inversion1nstd166human GRCh37.p13 chr6: 94,532,001-117,422,619 , GRCh38.p12 chr6: 93,822,283-117,101,456 , CRYBG1, 284 more genes
    nsv3924741copy number variation1nstd102humanPathogenic GRCh37 chr6: 106,951,594-126,102,365 , GRCh38 chr6: 106,503,719-125,781,219 , NCBI36 chr6: 107,058,287-126,144,058 LOC105377979, LOC105377936, 266 more genes
    nsv3924576copy number variation1nstd102humanPathogenic NCBI36 chr6: 97,164,591-122,524,393 , GRCh38 chr6: 96,609,994-122,161,548 , GRCh37 chr6: 97,057,870-122,482,694 TUBE1, PLN, 318 more genes
    nsv3924238copy number variation1nstd102humanUncertain significance NCBI36 chr6: 110,448,454-111,628,607 , GRCh38 chr6: 110,020,558-111,200,711 , GRCh37 chr6: 110,341,761-111,521,914 RNU6-906P, DDO, 30 more genes
    nsv3920683copy number variation1nstd102humanPathogenic NCBI36 chr6: 109,372,795-132,430,553 , GRCh37 chr6: 109,266,102-132,388,860 , GRCh38 chr6: 108,944,899-132,067,720 SSXP10, TRE-CTC1-7, 298 more genes
    nsv3919989copy number variation1nstd102humanUncertain significance NCBI36 chr6: 110,694,754-111,314,876 , GRCh37.p13 chr6: 110,588,061-111,208,183 , GRCh38.p12 chr6: 110,266,858-110,886,980 LOC105377940, LOC105377936, 18 more genes
    nsv3919897copy number variation1nstd102humanPathogenic NCBI36 chr6: 103,834,033-114,362,096 , GRCh37 chr6: 103,727,340-114,255,403 , GRCh38 chr6: 103,279,465-113,934,239 HACE1, RNU6-1144P, 174 more genes
    nsv3919111copy number variation1nstd102humanPathogenic GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637 RNU6-770P, MAP3K5-AS2, 810 more genes
    nsv3914025copy number variation1nstd102humanPathogenic NCBI36 chr6: 107,798,038-116,255,339 , GRCh38 chr6: 107,370,141-115,827,482 , GRCh37 chr6: 107,691,345-116,148,646 TRAF3IP2-AS1, RPS12P13, 139 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