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 135

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5558253sequence alteration1nstd206human GRCh38 chr4: 120,373,769-143,797,136 , GRCh37.p13 chr4: 121,294,924-144,718,289 , IL15, 218 more genes
    nsv5353195translocation1nstd200human GRCh38 chr4: 139,426,767-139,426,767 , GRCh38 chr4: 139,426,874-139,426,874 , GRCh37.p13 chr4: 140,347,921-140,347,921 , GRCh37.p13 chr4: 140,348,028-140,348,028 LOC100421868
    nsv5332228translocation1nstd200human GRCh37 chr4: 140,347,921-140,347,921 , GRCh37 chr4: 140,348,028-140,348,028 , GRCh38.p12 chr4: 139,426,767-139,426,767 , GRCh38.p12 chr4: 139,426,874-139,426,874 LOC100421868
    nsv5324341inversion1nstd204human GRCh37.p13 chr4: 137,941,712-143,237,910 , GRCh38.p13 chr4: 137,020,558-142,316,757 , ELF2, 68 more genes
    nsv5316524copy number variation1nstd204human GRCh38.p13 chr4: 139,417,099-139,426,335 , GRCh37.p13 chr4: 140,338,253-140,347,489 LOC100421868
    nsv5234451copy number variation1nstd204human GRCh38.p13 chr4: 139,417,468-139,425,620 , GRCh37.p13 chr4: 140,338,622-140,346,774 LOC100421868
    nsv4873391inversion1nstd200human GRCh37 chr4: 137,941,721-143,237,901 , GRCh38.p12 chr4: 137,020,567-142,316,748 , MAML3, 68 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4674743copy number variation1nstd102humanPathogenic GRCh37 chr4: 137,901,978-141,527,647 , GRCh38.p12 chr4: 136,980,824-140,606,493 RAB33B-AS1, PPP1R14BP3, 56 more genes
    nsv4674499copy number variation1nstd102humanPathogenic GRCh37 chr4: 139,531,815-146,095,109 , GRCh38.p12 chr4: 138,610,661-145,173,957 GUSBP5, LOC100287014, 77 more genes
    nsv4674465copy number variation1nstd102humanLikely benign GRCh37 chr4: 140,024,115-140,457,430 , GRCh38.p12 chr4: 139,102,961-139,536,276 RNU6-1214P, RN7SL311P, 12 more genes
    nsv4596915copy number variation1nstd183human GRCh37 chr4: 140,299,152-140,404,741 , GRCh38.p12 chr4: 139,377,998-139,483,587 , LOC100421868, 3 more genes
    nsv4456879copy number variation1nstd102humanUncertain significance GRCh37 chr4: 134,054,911-142,601,496 , GRCh38.p12 chr4: 133,133,756-141,680,343 NOCT, IL15, 81 more genes
    nsv4456498copy number variation1nstd102humanUncertain significance GRCh37 chr4: 140,333,549-140,417,276 , GRCh38.p12 chr4: 139,412,395-139,496,122 RAB33B, LOC100421868, 2 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