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 41

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2763832copy number variation300estd203human NCBI36 chr4: 9,802,525-9,848,395 , GRCh37.p13 chr4: 10,193,427-10,239,297 , GRCh38.p12 chr4: 10,191,803-10,237,673 LOC100129344
    esv2763673copy number variation70estd203human NCBI36 chr20: 52,070,481-52,101,533 , GRCh37.p13 chr20: 52,637,074-52,668,126 , GRCh38.p12 chr20: 54,020,535-54,051,587 BCAS1
    esv2761895copy number variation1estd203human NCBI36 chr16: 6,517,390-6,544,183 , GRCh37.p13 chr16: 6,577,389-6,604,182 , GRCh38.p12 chr16: 6,527,388-6,554,181 RBFOX1
    esv2763690copy number variation46estd203human NCBI36 chr21: 22,568,394-22,591,163 , GRCh37.p13 chr21|NW_003315968.1: 178,433-201,198 , GRCh37.p13 chr21: 23,646,523-23,669,292 , GRCh38.p12 chr21: 22,274,203-22,296,972 , GRCh38.p12 chr21|NW_003315968.2: 178,432-201,197 LOC107985508
    esv2763768copy number variation81estd203human NCBI36 chr3: 52,998,251-53,020,965 , GRCh37.p13 chr3: 53,023,211-53,045,925 , GRCh38.p12 chr3: 52,989,195-53,011,909 SFMBT1
    esv2761883copy number variation1estd203human NCBI36 chr15: 91,942,611-91,965,321 , GRCh37.p13 chr15: 94,141,607-94,164,317 , GRCh38.p12 chr15: 93,598,378-93,621,088 LOC107983974
    esv2762298copy number variation79estd203human NCBI36 chr1: 111,171,895-111,193,590 , GRCh37.p13 chr1: 111,370,372-111,392,067 , GRCh38.p12 chr1: 110,827,750-110,849,445 NRBF2P3
    esv2763635copy number variation47estd203human NCBI36 chr2: 180,119,248-180,133,937 , GRCh37.p13 chr2: 180,411,003-180,425,692 , GRCh38.p12 chr2: 179,546,276-179,560,965 ZNF385B
    esv2763254copy number variation37estd203human NCBI36 chr2: 183,792,398-183,805,765 , GRCh37.p13 chr2: 184,084,153-184,097,520 , GRCh38.p12 chr2: 183,219,425-183,232,792
    esv2762899copy number variation78estd203human NCBI36 chr18: 38,303,048-38,312,393 , GRCh37.p13 chr18: 40,049,050-40,058,395 , GRCh38.p12 chr18: 42,469,085-42,478,430 LINC00907
    esv2764004copy number variation13estd203human NCBI36 chr7: 16,666,972-16,668,369 , GRCh37.p13 chr7: 16,700,447-16,701,844 , GRCh38.p12 chr7: 16,660,822-16,662,219 BZW2
    esv2764021copy number variation96estd203human NCBI36 chr7: 141,404,060-141,441,975 , GRCh37.p13 chr7|NW_003571040.1: 199,742-237,657 , GRCh37.p13 chr7: 141,757,591-141,795,506 , GRCh38.p12 chr7: 142,057,791-142,095,706 , GRCh38.p12 chr7|NT_187562.1: 19,671-57,586 MGAM
    esv2762092copy number variation1estd203human NCBI36 chr21: 15,732,981-15,734,753 , GRCh37.p13 chr21: 16,811,110-16,812,882 , GRCh38.p12 chr21: 15,438,791-15,440,563 LOC101927745
    esv2763894copy number variation77estd203human NCBI36 chr5: 15,767,022-15,916,332 , GRCh37.p13 chr5: 15,714,022-15,863,332 , GRCh38.p12 chr5: 15,713,913-15,863,223 FBXL7, LOC107986343
    esv2760244copy number variation170estd203human NCBI36 chr11: 18,891,410-18,936,569 , GRCh37.p13 chr11: 18,934,834-18,979,993 , GRCh38.p12 chr11: 18,913,287-18,958,446 MRGPRX1, MRGPRX11P
    esv2760755copy number variation49estd203human NCBI36 chr12: 27,532,181-27,548,428 , GRCh37.p13 chr12: 27,640,914-27,657,161 , GRCh38.p12 chr12: 27,487,981-27,504,228 SMCO2, RARS1P1
    esv2762943copy number variation56estd203human NCBI36 chr19: 40,537,990-40,553,688 , GRCh37.p13 chr19: 35,846,150-35,861,848 , GRCh38.p12 chr19: 35,355,248-35,370,946 FFAR3, GPR42
    esv2760599copy number variation6estd203human NCBI36 chr11: 25,143,560-26,116,026 , GRCh37.p13 chr11: 25,186,984-26,159,450 , GRCh38.p12 chr11: 25,165,438-26,137,903 RPL36AP40, LOC100533706, 2 more genes
    esv2764112copy number variation42estd203human NCBI36 chr8: 16,241,562-16,754,911 , GRCh37.p13 chr8: 16,197,191-16,710,540 , GRCh38.p12 chr8: 16,339,682-16,853,031 MRPL49P2, LOC101929028, 1 more genes
    esv2761948copy number variation1estd203human NCBI36 chr17: 16,809,286-16,861,293 , GRCh37.p13 chr17: 16,868,561-16,920,568 , GRCh38.p12 chr17: 16,965,247-17,017,254 TNFRSF13B, LOC284191, 1 more genes
    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