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 298

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112780copy number variation1nstd102humanPathogenic GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538 LOC105371009, ST8SIA2, 149 more genes
    nsv5973246inversion1nstd209human GRCh38 chr15: 97,535,582-101,746,493 , GRCh37.p13 chr15: 98,078,812-102,286,696 , ALDH1A3, 71 more genes
    nsv5695814mobile element insertion1nstd211human GRCh38 chr15: 101,282,986-101,282,986 , GRCh37.p13 chr15: 101,823,191-101,823,191 SNRPA1
    nsv5647866insertion1nstd207human GRCh38 chr15: 101,282,976-101,282,976 , GRCh37.p13 chr15: 101,823,181-101,823,181 SNRPA1
    nsv5431261mobile element insertion1nstd206human GRCh38 chr15: 101,282,986-101,282,991 , GRCh37.p13 chr15: 101,823,191-101,823,196 SNRPA1
    nsv5317817copy number variation1nstd204human GRCh38.p13 chr15: 101,295,524-101,295,781 , GRCh37.p13 chr15: 101,835,729-101,835,986 SNRPA1
    nsv5309609copy number variation1nstd204human GRCh38.p13 chr15: 101,100,037-101,575,686 , GRCh37.p13 chr15: 101,640,242-102,115,889 , LOC105371026, 9 more genes
    nsv5279124copy number variation1nstd204human GRCh38.p13 chr15: 101,252,901-101,325,400 , GRCh37.p13 chr15: 101,793,106-101,865,605 PCSK6, SELENOS, 3 more genes
    nsv5268015copy number variation1nstd204human GRCh38.p13 chr15: 101,250,307-101,285,764 , GRCh37.p13 chr15: 101,790,512-101,825,969 LOC107984727, SNRPA1, 2 more genes
    nsv5155332mobile element insertion1nstd203human GRCh38 chr15: 101,282,976-101,282,986 , GRCh37.p13 chr15: 101,823,181-101,823,191 SNRPA1
    nsv5148802mobile element insertion1nstd203human GRCh38 chr15: 101,294,071-101,294,080 , GRCh37.p13 chr15: 101,834,276-101,834,285 SNRPA1
    nsv5009283copy number variation1nstd200human GRCh38 chr15: 101,295,637-101,360,199 , GRCh37.p13 chr15: 101,835,842-101,900,404 PCSK6-AS1, LOC100507472, 2 more genes
    nsv5009282copy number variation1nstd200human GRCh38 chr15: 101,269,543-101,602,834 , GRCh37.p13 chr15: 101,809,748-102,143,037 , SELENOS, 7 more genes
    nsv5009280copy number variation1nstd200human GRCh38 chr15: 101,119,482-101,519,791 , GRCh37.p13 chr15: 101,659,687-102,059,994 , LOC105371026, 8 more genes
    nsv5002784copy number variation1nstd200human GRCh38 chr15: 101,294,268-101,294,503 , GRCh37.p13 chr15: 101,834,473-101,834,708 SNRPA1
    nsv5002780copy number variation1nstd200human GRCh38 chr15: 101,100,045-101,575,680 , GRCh37.p13 chr15: 101,640,250-102,115,883 , SNRPCP18, 9 more genes
    nsv4856615copy number variation1nstd200human GRCh37 chr15: 101,640,251-102,115,883 , GRCh38.p12 chr15: 101,100,046-101,575,680 , LOC105371026, 9 more genes
    nsv4854286copy number variation1nstd200human GRCh37 chr15: 101,779,792-102,137,111 , GRCh38.p12 chr15: 101,239,587-101,596,908 , SNRPCP18, 8 more genes
    nsv4729524copy number variation1nstd102humanUncertain significance GRCh37 chr15: 100,853,021-102,429,112 , GRCh38.p12 chr15: 100,312,816-101,888,909 LOC105371021, OR4F28P, 42 more genes
    nsv4729418copy number variation1nstd102humanLikely benign GRCh37 chr15: 101,683,593-102,270,458 , GRCh38.p12 chr15: 101,143,388-101,730,255 SELENOS, LOC107987228, 12 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