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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5896500copy number variation1nstd209human GRCh38 chr3: 171,525,972-180,293,041 , GRCh37.p13 chr3: 171,243,761-180,010,829 , RNU6-1120P, 95 more genes
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5225286copy number variation1nstd204human GRCh38.p13 chr3: 179,580,197-179,581,396 , GRCh37.p13 chr3: 179,297,985-179,299,184 ACTL6A
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4924917copy number variation1nstd200human GRCh38 chr3: 179,578,449-179,602,925 , GRCh37.p13 chr3: 179,296,237-179,320,713 NDUFB5, MRPL47, 1 more genes
    nsv4805039copy number variation1nstd200human GRCh37 chr3: 179,296,237-179,320,713 , GRCh38.p12 chr3: 179,578,449-179,602,925 NDUFB5, ACTL6A, 1 more genes
    nsv4728751copy number variation1nstd102humanPathogenic GRCh37 chr3: 179,016,729-181,527,320 , GRCh38.p12 chr3: 179,298,941-181,809,532 PEX5L, NDUFB5, 33 more genes
    nsv4674680copy number variation1nstd102humanPathogenic GRCh37 chr3: 169,617,690-190,593,854 , GRCh38.p12 chr3: 169,899,902-190,876,065 RNU6-1120P, LOC105374262, 323 more genes
    nsv4587905copy number variation2nstd183human GRCh37 chr3: 179,291,129-179,292,190 , GRCh38.p12 chr3: 179,573,341-179,574,402 ACTL6A
    nsv4436681copy number variation1nstd102humanUncertain significance GRCh37 chr3: 178,869,440-179,400,345 , GRCh38.p12 chr3: 179,151,652-179,682,557 NDUFB5, LRRFIP1P1, 11 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv3962224copy number variation1nstd168human GRCh38 chr3: 179,545,526-179,572,890 , GRCh37.p13 chr3: 179,263,314-179,290,678 ACTL6A
    nsv3922385copy number variation1nstd102humanPathogenic NCBI36 chr3: 177,369,007-199,329,651 , GRCh37 chr3: 175,886,313-197,845,254 , GRCh38 chr3: 176,168,525-198,118,383 LINC02053, RTP4, 414 more genes
    nsv3921569copy number variation1nstd102humanUncertain significance NCBI36 chr3: 180,678,889-180,831,872 , GRCh37.p13 chr3: 179,196,195-179,349,178 , GRCh38.p12 chr3: 179,478,407-179,631,390 NDUFB5, ACTL6A, 1 more genes
    nsv3920662copy number variation1nstd102humanPathogenic NCBI36 chr3: 178,729,187-199,321,446 , GRCh37.p13 chr3: 177,246,493-197,837,049 , GRCh38.p12 chr3: 177,528,705-198,110,178 RN7SKP265, RPL24P6, 401 more genes
    nsv3918982copy number variation1nstd102humanPathogenic GRCh37 chr3: 167,885,356-197,837,049 , NCBI36 chr3: 169,368,050-199,321,446 , GRCh38 chr3: 168,167,568-198,110,178 EIF4G1, LOC105374248, 515 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 LINC02614, LINC02054, 1469 more genes
    nsv3918692copy number variation1nstd102humanPathogenic GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833 LOC105374179, LINC02038, 785 more genes
    nsv3918149copy number variation1nstd102humanPathogenic GRCh37 chr3: 155,836,230-197,851,986 , GRCh38 chr3: 156,118,441-198,125,115 , NCBI36 chr3: 157,318,924-199,336,383 LINC02031, PCBP2P4, 647 more genes
    nsv3918066copy number variation1nstd102humanPathogenic GRCh38 chr3: 152,100,512-198,118,383 , NCBI36 chr3: 153,300,991-199,329,651 , GRCh37 chr3: 151,818,301-197,845,254 LOC105374260, LOC105374174, 696 more genes
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