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 33

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv471658copy number variation79nstd32human GRCh38.p12 chr21: 9,886,669-10,112,700 , NCBI34 chr9: 43,184,378-43,416,941 , GRCh37.p13 chr9: 45,448,738-46,055,884 LOC105372733, LOC105372734, 1 more genes
    nsv471599copy number variation36nstd32human NCBI34 chrX: 423,855-595,665 , GRCh37.p13 chrX: 481,676-653,486 , GRCh38.p12 chrX: 520,941-692,751 SHOX, KRT18P53, 1 more genes
    nsv471637copy number variation5nstd32human GRCh38.p12 chr6: 47,339,291-47,493,663 , NCBI34 chr6: 47,353,863-47,508,235 , GRCh37.p13 chr6: 47,307,027-47,461,399 CD2AP, LOC105375082, 1 more genes
    nsv471707copy number variation7nstd32human GRCh38.p12 chr21: 13,383,154-13,535,153 , NCBI34 chr21: 13,677,346-13,829,345 , GRCh37.p13 chr21: 14,755,475-14,907,474 VN1R8P, GTF2IP2, 3 more genes
    nsv471620copy number variation13nstd32human GRCh37.p13 chr3: 84,880,814-85,031,486 , GRCh38.p12 chr3: 84,831,663-84,982,335 , NCBI34 chr3: 84,801,715-84,952,387 , GRCh38.p12 chr3|NW_018654711.1: 31,696-175,849 CADM2, LINC00971, 2 more genes
    nsv471677copy number variation43nstd32human NCBI34 chr1: 103,532,648-103,647,985 , GRCh38.p12 chr1: 103,635,373-103,750,710 , GRCh37.p13 chr1: 104,177,995-104,293,332 AMY1A, AMY1B, 3 more genes
    nsv471691copy number variation19nstd32human NCBI34 chr16: 22,446,888-22,652,575 , GRCh38.p12 chr16: 22,469,014-22,674,701 , GRCh37.p13 chr16: 22,480,335-22,686,022 SMG1P1, OTOAP1, 3 more genes
    nsv471701copy number variation15nstd32human GRCh37.p13 chr17: 45,511,583-45,698,942 , NCBI34 chr17: 45,986,221-46,173,580 , GRCh38.p12 chr17: 47,434,217-47,621,576 NPEPPS, EFCAB13, 2 more genes
    nsv471692copy number variation24nstd32human NCBI34 chr16: 32,585,216-32,745,821 , GRCh38.p12 chr16: 32,537,598-32,698,203 , GRCh37.p13 chr16: 32,548,919-32,709,524 TP53TG3, FAM153DP, 2 more genes
    nsv471698copy number variation76nstd32human GRCh37.p13 chr17: 44,079,479-44,378,253 , NCBI34 chr17: 44,554,955-44,853,669 , GRCh38.p12 chr17: 46,002,113-46,300,887 MAPT, LRRC37A, 7 more genes
    nsv471614copy number variation17nstd32human NCBI34 chr1: 193,957,770-194,243,489 , GRCh38.p12 chr1: 196,700,381-196,986,100 , GRCh37.p13 chr1: 196,669,511-196,955,230 CFH, CFHR1, 6 more genes
    nsv471661copy number variation135nstd32human NCBI34 chr9: 64,805,733-65,060,890 , GRCh38.p12 chr9: 63,542,269-63,776,777 , GRCh37.p13 chr9: 68,138,003-68,372,511 CDK2AP2P3, RPL7AP46, 5 more genes
    nsv471595copy number variation34nstd32human NCBI34 chr22: 19,757,626-19,940,794 , GRCh38.p12 chr22: 21,078,783-21,261,951 , GRCh37.p13 chr22: 21,433,072-21,616,240 E2F6P2, BCRP2, 6 more genes
    nsv471625copy number variation25nstd32human GRCh38.p12 chr4: 69,250,956-69,410,069 , GRCh37.p13 chr4: 70,116,674-70,275,787 , NCBI34 chr4: 70,432,219-70,591,332 UGT2B28, UGT2B25P, 6 more genes
    nsv471673copy number variation171nstd32human NCBI34 chr14: 104,194,660-104,731,664 , GRCh38.p12 chr14: 105,786,368-106,303,735 , GRCh37.p13 chr14: 106,252,705-106,759,988 , GRCh38.p12 chr14|NT_187600.1: 224,416-1,214,078 IGH, IGHD, 169 more genes
    nsv471594copy number variation65nstd32human NCBI34 chr22: 16,933,332-17,244,196 , GRCh38.p12 chr22: 18,076,012-18,882,129 , GRCh37.p13 chr22: 18,558,778-18,869,642 GGT3P, USP18, 29 more genes
    nsv471660copy number variation141nstd32human NCBI34 chr9: 62,937,487-63,676,740 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr: NaN-NaN 0
    nsv471657copy number variation33nstd32human NCBI34 chr9: 42,363,623-42,769,926 , GRCh38.p12 chr9: 61,822,142-62,139,850 , GRCh37.p13 chr: NaN-NaN , FAM27C, 9 more genes
    nsv471623copy number variation41nstd32human GRCh38.p12 chr4: 9,322,917-9,592,435 , GRCh37.p13 chr4: 9,324,643-9,594,059 , NCBI34 chr4: 9,041,260-9,344,942 OR7E84P, USP17L6P, 23 more genes
    nsv471656copy number variation8nstd32human NCBI34 chr9: 41,840,001-42,021,335 , GRCh37.p13 chr: NaN-NaN , GRCh38.p12 chr: NaN-NaN 0
    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