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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975449inversion1nstd209human GRCh38 chr8: 70,630,457-73,057,328 , GRCh37.p13 chr8: 71,542,692-73,969,563 , EYA1, 23 more genes
    nsv5037389inversion1nstd200human GRCh38 chr8: 70,182,890-71,982,045 , GRCh37.p13 chr8: 71,095,125-72,894,280 LACTB2, RPS18P11, 20 more genes
    nsv4729578copy number variation1nstd102humanUncertain significance GRCh37 chr8: 71,244,655-71,685,822 , GRCh38.p12 chr8: 70,332,420-70,773,587 LOC105375890, LACTB2-AS1, 10 more genes
    nsv4675545copy number variation1nstd102humanUncertain significance GRCh37 chr8: 70,848,713-71,632,067 , GRCh38.p12 chr8: 69,936,478-70,719,832 SDCBPP2, RNY3P14, 16 more genes
    nsv4599291copy number variation1nstd183human GRCh37 chr8: 71,461,521-71,631,870 , GRCh38.p12 chr8: 70,549,286-70,719,635 TRAM1, LACTB2, 3 more genes
    nsv4496990mobile element insertion1nstd166human GRCh37.p13 chr8: 71,565,076-71,565,076 , GRCh38.p12 chr8: 70,652,841-70,652,841 LACTB2, LACTB2-AS1, 1 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4455590copy number variation1nstd102humanUncertain significance GRCh37 chr8: 71,475,270-71,849,895 , GRCh38.p12 chr8: 70,563,035-70,937,660 TRAM1, RN7SL19P, 3 more genes
    nsv4365779copy number variation1nstd173human GRCh37 chr8: 71,557,604-71,671,973 , GRCh38.p12 chr8: 70,645,369-70,759,738 LACTB2, LACTB2-AS1, 2 more genes
    nsv4365318copy number variation1nstd173human GRCh37 chr8: 71,529,266-71,663,110 , GRCh38.p12 chr8: 70,617,031-70,750,875 LACTB2, XKR9, 2 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
    nsv4332950sequence alteration1nstd166human GRCh37.p13 chr8: 71,555,538-71,622,803 , GRCh38.p12 chr8: 70,643,303-70,710,568 LACTB2, LACTB2-AS1, 2 more genes
    nsv4332062inversion1nstd166human GRCh37.p13 chr8: 70,438,609-99,073,700 , GRCh38.p12 chr8: 69,526,374-98,061,472 , FTH1P11, 375 more genes
    nsv4318272inversion1nstd166human GRCh37.p13 chr8: 51,271,211-76,167,888 , GRCh38.p12 chr8: 50,358,651-75,255,653 , ASPH, 341 more genes
    nsv4164126copy number variation1nstd166human GRCh37.p13 chr8: 71,551,930-71,564,991 , GRCh38.p12 chr8: 70,639,695-70,652,756 LACTB2, LACTB2-AS1, 1 more genes
    nsv3924445copy number variation1nstd102humanUncertain significance GRCh37 chr8: 71,537,891-71,716,890 , GRCh38 chr8: 70,625,656-70,804,655 , NCBI36 chr8: 71,700,445-71,879,444 XKR9, LACTB2, 2 more genes
    nsv3923937copy number variation1nstd102humanPathogenic NCBI36 chr8: 69,562,804-72,550,966 , GRCh37 chr8: 69,400,250-72,388,412 , GRCh38 chr8: 68,488,015-71,476,177 RNY3P14, RPS15AP25, 37 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 LOC112268023, RPL23AP96, 2105 more genes
    nsv3923011copy number variation1nstd102humanPathogenic GRCh38 chr8: 66,171,669-93,505,509 , GRCh37 chr8: 67,083,904-94,517,737 , NCBI36 chr8: 67,246,458-94,586,913 CA3, HAUS1P3, 353 more genes
    nsv3922631copy number variation1nstd102humanPathogenic GRCh38 chr8: 61,691,800-82,537,696 , NCBI36 chr8: 62,766,913-83,612,486 , GRCh37 chr8: 62,604,359-83,449,931 NCOA2, LOC107986893, 284 more genes
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