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 161

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv442908copy number variation238nstd22human NCBI35 chr1: 72,480,937-72,523,169 , GRCh37.p13 chr1: 72,768,916-72,811,148 , GRCh38.p12 chr1: 72,303,233-72,345,465 , GRCh38.p12 chr1|NW_018654707.1: 15,500-66,690 LOC105378797
    nsv442901copy number variation79nstd22human NCBI35 chr4: 34,601,591-34,646,749 , GRCh37.p13 chr4|NW_003315915.1: 269,732-314,890 , GRCh37.p13 chr4: 34,779,025-34,824,183 , GRCh38.p12 chr4: 34,777,403-34,822,561 , GRCh38.p12 chr4|NW_003315915.1: 269,732-314,890 LOC105378262
    nsv442969copy number variation206nstd22human NCBI35 chr5: 177,090,005-177,131,055 , GRCh37.p13 chr5: 177,157,399-177,198,449 , GRCh38.p12 chr5: 177,730,398-177,771,448 FAM153A
    nsv442690copy number variation115nstd22human NCBI35 chr15: 22,029,857-22,065,565 , GRCh37.p13 chr15: 24,478,764-24,514,472 , GRCh38.p12 chr15: 24,233,617-24,269,325 LOC105370733
    nsv442776copy number variation260nstd22human NCBI35 chr20: 1,509,580-1,541,893 , GRCh37.p13 chr20: 1,561,580-1,593,893 , GRCh38.p12 chr20: 1,580,934-1,613,247 SIRPB1
    nsv442187copy number variation52nstd22human NCBI35 chr7: 141,222,827-141,245,092 , GRCh37.p13 chr7|NW_003571040.1: 211,794-234,059 , GRCh37.p13 chr7: 141,769,643-141,791,908 , GRCh38.p12 chr7: 142,069,843-142,092,108 , GRCh38.p12 chr7|NT_187562.1: 31,723-53,988 MGAM
    nsv442803copy number variation170nstd22human NCBI35 chr2: 97,599,265-97,620,228 , GRCh37.p13 chr2: 98,140,747-98,161,710 , GRCh38.p12 chr2: 97,524,284-97,545,247 ANKRD36B
    nsv442759copy number variation270nstd22human NCBI35 chr19: 8,256,197-8,271,067 , GRCh37.p13 chr19: 8,350,197-8,365,067 , GRCh38.p12 chr19: 8,285,313-8,300,183 CD320
    nsv442294copy number variation267nstd22human NCBI35 chr7: 157,617,027-157,631,641 , GRCh37.p13 chr7: 158,117,551-158,132,165 , GRCh38.p12 chr7: 158,324,859-158,339,473 , GRCh38.p12 chr7|NT_187560.1: 137,702-152,355 PTPRN2
    nsv442150copy number variation117nstd22human NCBI35 chr7: 133,242,450-133,256,409 , GRCh37.p13 chr7: 133,785,195-133,799,154 , GRCh38.p12 chr7: 134,100,442-134,114,401
    nsv442518copy number variation92nstd22human NCBI35 chr8: 58,279,104-58,292,579 , GRCh37.p13 chr8: 58,116,550-58,130,025 , GRCh38.p12 chr8: 57,203,991-57,217,466 LINC01606
    nsv442587copy number variation165nstd22human NCBI35 chr10: 81,475,459-81,486,935 , GRCh37.p13 chr10: 81,485,267-81,496,755 , GRCh38.p12 chr10: 79,725,511-79,736,999 NUTM2B-AS1
    nsv442658copy number variation36nstd22human NCBI35 chr12: 126,100,573-126,110,468 , GRCh37.p13 chr12: 127,575,693-127,585,588 , GRCh38.p12 chr12: 127,091,148-127,101,043 , GRCh38.p12 chr12|NW_019805499.1: 37,672-47,567 LOC107984449
    nsv442782copy number variation156nstd22human NCBI35 chr2: 87,426,037-87,434,600 , GRCh37.p13 chr2: 87,514,379-87,522,942 , GRCh38.p12 chr2: 87,287,256-87,295,819 LOC107985908
    nsv442352copy number variation82nstd22human NCBI35 chr1: 165,965,632-165,973,424 , GRCh37.p13 chr1: 169,233,974-169,241,766 , GRCh38.p12 chr1: 169,264,736-169,272,528 NME7
    nsv442256copy number variation163nstd22human NCBI35 chr7: 153,830,819-153,838,481 , GRCh37.p13 chr7: 154,393,171-154,400,833 , GRCh38.p12 chr7: 154,601,461-154,609,123 DPP6
    nsv442666copy number variation87nstd22human NCBI35 chr13: 31,430,622-31,436,423 , GRCh37.p13 chr13: 32,532,622-32,538,423 , GRCh38.p12 chr13: 31,958,485-31,964,286 EEF1DP3
    nsv442506copy number variation57nstd22human NCBI35 chr8: 24,201,375-24,207,011 , GRCh37.p13 chr8: 24,145,430-24,151,066 , GRCh38.p12 chr8: 24,287,917-24,293,553 ADAM28
    nsv442664copy number variation62nstd22human NCBI35 chr13: 24,407,846-24,413,343 , GRCh37.p13 chr13: 25,509,846-25,515,343 , GRCh38.p12 chr13: 24,935,708-24,941,205 TPTE2P1
    nsv442649copy number variation74nstd22human NCBI35 chr12: 69,158,942-69,164,294 , GRCh37.p13 chr12: 70,872,675-70,878,027 , GRCh38.p12 chr12: 70,478,895-70,484,247
    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