U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 1412

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv9999copy number variation1estd20human NCBI36 chr1: 187,250,900-187,304,747 , GRCh37.p13 chr1: 188,984,277-189,038,124 , GRCh38.p12 chr1: 189,015,146-189,068,993 CLPTM1LP1
    esv11812copy number variation28estd20human NCBI36 chr20: 1,500,338-1,544,222 , GRCh37.p13 chr20: 1,552,338-1,596,222 , GRCh38.p12 chr20: 1,571,692-1,615,576 SIRPB1
    esv17112copy number variation4estd20human NCBI36 chr15: 18,462,131-18,495,962 , GRCh37.p13 chr15: 20,202,117-20,235,948 , GRCh38.p12 chr15: 19,996,864-20,030,695 FAM30B
    esv14847copy number variation19estd20human NCBI36 chr15: 82,861,600-82,890,050 , GRCh37.p13 chr15: 85,060,596-85,089,046 , GRCh38.p12 chr15: 84,517,365-84,545,815 UBE2Q2P1
    esv19221copy number variation22estd20human NCBI36 chr10: 47,875,346-47,900,761 , GRCh37.p13 chr10|NW_003871068.1: 1,729,722-1,755,137 , GRCh37.p13 chr10: 48,255,340-48,280,755 , GRCh38.p12 chr10: 47,458,607-47,484,022 ANXA8
    esv16042copy number variation5estd20human NCBI36 chr17: 6,042,627-6,067,580 , GRCh37.p13 chr17: 6,101,903-6,126,856 , GRCh38.p12 chr17: 6,198,583-6,223,536 RNU6-1264P
    esv15136copy number variation40estd20human NCBI36 chr10: 56,116,082-56,139,577 , GRCh37.p13 chr10: 56,446,076-56,469,571 , GRCh38.p12 chr10: 54,686,316-54,709,811 PCDH15
    esv18824copy number variation22estd20human NCBI36 chr10: 18,881,143-18,902,755 , GRCh37.p13 chr10: 18,841,137-18,862,749 , GRCh38.p12 chr10: 18,552,208-18,573,820 NSUN6
    esv15201copy number variation12estd20human NCBI36 chr2: 97,221,105-97,241,816 , GRCh37.p13 chr2: 97,857,378-97,878,089 , GRCh38.p12 chr2: 97,191,641-97,212,352 ANKRD36
    esv11909copy number variation8estd20human NCBI36 chr7: 149,493,466-149,513,725 , GRCh37.p13 chr7: 149,862,533-149,882,792 , GRCh38.p12 chr7: 150,165,444-150,185,703 ACTR3C
    esv10911copy number variation11estd20human NCBI36 chr11: 7,769,434-7,789,226 , GRCh37.p13 chr11: 7,812,858-7,832,650 , GRCh38.p12 chr11: 7,791,311-7,811,103 , GRCh38.p12 chr11|NT_187583.1: 12,179-31,971 , GRCh38.p12 chr11|NW_011332695.1: 12,179-31,973 OR5P2
    esv19413copy number variation34estd20human NCBI36 chr15: 82,606,345-82,625,912 , GRCh37.p13 chr15: 84,815,341-84,834,908 , GRCh38.p12 chr15: 84,146,589-84,166,156 DNM1P41
    esv14265copy number variation1estd20human NCBI36 chr11: 70,507,951-70,527,201 , GRCh37.p13 chr11|NW_004070871.1: 613,470-632,720 , GRCh37.p13 chr11: 70,830,303-70,849,553 , GRCh38.p12 chr11: 71,119,257-71,138,507 SHANK2
    esv10276copy number variation23estd20human NCBI36 chr7: 126,301,909-126,320,398 , GRCh37.p13 chr7: 126,514,673-126,533,162 , GRCh38.p12 chr7: 126,874,619-126,893,108 GRM8
    esv10316copy number variation31estd20human NCBI36 chr7: 64,657,580-64,675,115 , GRCh37.p13 chr7|NW_004775430.1: 8,063-25,598 , GRCh37.p13 chr7: 65,020,145-65,037,680 , GRCh38.p12 chr7: 65,555,232-65,572,767 LOC101929322
    esv13139copy number variation5estd20human NCBI36 chr7: 102,135,311-102,152,748 , GRCh37.p13 chr7: 102,348,075-102,365,512 , GRCh38.p12 chr7: 102,707,628-102,725,065 RASA4DP
    esv12068copy number variation14estd20human NCBI36 chr7: 100,419,557-100,436,582 , GRCh37.p13 chr7: 100,632,837-100,649,862 , GRCh38.p12 chr7: 100,989,556-101,006,581 MUC12
    esv10448copy number variation15estd20human NCBI36 chr6: 33,131,047-33,147,969 , GRCh37.p13 chr6: 33,023,069-33,039,991 , GRCh37.p13 chr6|NT_167247.1: 4,359,938-4,376,864 , GRCh37.p13 chr6|NT_167249.1: 4,503,607-4,520,495 , GRCh37.p13 chr6|NT_167244.1: 4,309,883-4,326,810 , GRCh37.p13 chr6|NT_167245.1: 4,304,407-4,321,330 , GRCh38.p12 chr6: 33,055,292-33,072,214 , GRCh38.p12 chr6|NT_167247.2: 4,354,353-4,371,279 , GRCh38.p12 chr6|NT_167249.2: 4,504,309-4,521,197 , GRCh38.p12 chr6|NT_167245.2: 4,298,822-4,315,745 , GRCh38.p12 chr6|NT_167244.2: 4,359,967-4,376,894 HLA-DPA1
    esv13975copy number variation2estd20human NCBI36 chr18: 14,542,243-14,557,604 , GRCh37.p13 chr18: 14,552,243-14,567,604 , GRCh38.p12 chr18: 14,552,244-14,567,605 LOC105372004
    esv14583copy number variation30estd20human NCBI36 chr8: 1,328,300-1,343,560 , GRCh37.p13 chr8: 1,340,893-1,356,153 , GRCh38.p12 chr8: 1,392,727-1,407,987 , GRCh38.p12 chr8|NT_187654.1: 3,011-18,271 DLGAP2
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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