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 54

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3905717copy number variation1nstd102humanBenign GRCh37 chr15: 61,216,975-61,269,292 , GRCh38.p12 chr15: 60,924,776-60,977,093 RORA
    nsv4682863copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 61,328,907-61,398,869 , GRCh38.p12 chr15: 61,036,708-61,106,670 RORA, LOC107984805
    nsv3907025copy number variation1nstd102humanBenign GRCh37 chr15: 61,020,254-61,105,886 , GRCh38.p12 chr15: 60,728,055-60,813,687 RORA, RNA5SP397, 1 more genes
    nsv4728462copy number variation1nstd102humanUncertain significance GRCh37 chr1: 64,076,769-64,300,916 , GRCh38.p12 chr1: 63,611,098-63,835,245 ROR1, RN7SL130P, 3 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 H3P40, EEF1B2P1, 1616 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3901546copy number variation1nstd102humanPathogenic NCBI36 chr1: 59,057,865-86,336,882 , GRCh37 chr1: 59,285,277-86,564,294 , GRCh38 chr1: 58,819,605-86,098,611 ROR1, RNA5SP51, 333 more genes
    nsv3886551copy number variation1nstd102humanPathogenic GRCh37 chr1: 64,321,264-88,153,669 , GRCh38.p12 chr1: 63,855,593-87,687,986 ROR1, RNU6-1102P, 291 more genes
    nsv3884583copy number variation1nstd102humanPathogenic GRCh37 chr1: 61,351,024-79,583,933 , GRCh38.p12 chr1: 60,885,352-79,118,248 ROR1, MIR7156, 243 more genes
    nsv3903468copy number variation1nstd102humanPathogenic NCBI36 chr1: 59,870,760-76,969,150 , GRCh37 chr1: 60,098,172-77,196,562 , GRCh38 chr1: 59,632,500-76,730,877 ROR1, WLS, 219 more genes
    nsv3909388copy number variation1nstd102humanPathogenic GRCh37 chr1: 57,816,246-71,791,607 , GRCh38 chr1: 57,350,574-71,325,924 , NCBI36 chr1: 57,588,834-71,564,195 ROR1, RNU6-1031P, 193 more genes
    nsv4768338copy number variation1nstd102humanPathogenic GRCh37 chr1: 53,675,707-66,644,963 , GRCh38.p12 chr1: 53,210,035-66,179,280 ROR1, TALDO1P1, 201 more genes
    nsv4453663copy number variation1nstd102humanPathogenic GRCh37 chr1: 59,922,631-72,058,653 , GRCh38.p12 chr1: 59,456,959-71,592,970 ROR1, RNU6-387P, 170 more genes
    nsv3901841copy number variation1nstd102humanPathogenic GRCh38 chr1: 59,760,856-71,578,052 , NCBI36 chr1: 59,999,116-71,816,323 , GRCh37 chr1: 60,226,528-72,043,735 ROR1, MIR3116-2, 169 more genes
    nsv3895522copy number variation1nstd102humanPathogenic GRCh37 chr1: 54,092,945-64,714,537 , GRCh38 chr1: 53,627,272-64,248,854 , NCBI36 chr1: 53,865,533-64,487,125 ROR1, FGGY, 159 more genes
    nsv3901058copy number variation1nstd102humanPathogenic GRCh38 chr1: 60,473,800-70,944,955 , NCBI36 chr1: 60,712,060-71,183,226 , GRCh37 chr1: 60,939,472-71,410,638 ROR1, UBE2U, 150 more genes
    nsv3891330copy number variation1nstd102humanPathogenic NCBI36 chr1: 59,057,865-69,345,379 , GRCh37 chr1: 59,285,277-69,572,791 , GRCh38 chr1: 58,819,605-69,107,108 ROR1, RPS7P4, 148 more genes
    nsv3899878copy number variation1nstd102humanPathogenic GRCh37 chr15: 54,713,558-62,769,295 , GRCh38.p12 chr15: 54,421,360-62,477,096 RAB27A, RNF111, 120 more genes
    nsv7095627copy number variation1nstd102humanPathogenic GRCh37 chr1: 61,548,464-67,861,772 , GRCh38.p12 chr1: 61,082,792-67,396,089 ROR1, ALG6, 94 more genes
    nsv3921425copy number variation1nstd102humanPathogenic NCBI36 chr15: 55,647,440-61,098,667 , GRCh37 chr15: 57,860,148-63,311,614 , GRCh38 chr15: 57,567,950-63,019,415 MESTP2, HMGB1P51, 86 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