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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3903508copy number variation1nstd102humanLikely benign GRCh37 chr8: 71,549,662-71,647,145 , GRCh38.p12 chr8: 70,637,427-70,734,910 LACTB2, XKR9, 2 more genes
    nsv4455590copy number variation1nstd102humanUncertain significance GRCh37 chr8: 71,475,270-71,849,895 , GRCh38.p12 chr8: 70,563,035-70,937,660 LACTB2, TRAM1, 3 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 LACTB2, XKR9, 2 more genes
    nsv3894927copy number variation1nstd102humanUncertain significance GRCh37 chr8: 71,525,694-71,835,493 , GRCh38.p12 chr8: 70,613,459-70,923,258 LACTB2, RN7SL19P, 2 more genes
    nsv3913383copy number variation1nstd102humanUncertain significance NCBI36 chr8: 71,663,621-71,847,724 , GRCh37.p13 chr8: 71,501,067-71,685,170 , GRCh38.p12 chr8: 70,588,832-70,772,935 LACTB2, XKR9, 3 more genes
    nsv3914262copy number variation1nstd102humanPathogenic GRCh37 chr8: 63,143,195-74,140,021 , GRCh38 chr8: 62,230,636-73,227,786 , NCBI36 chr8: 63,305,749-74,302,575 LACTB2, RRS1, 151 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 LACTB2, RNY3P14, 37 more genes
    nsv6291265copy number variation1nstd102humanPathogenic GRCh37 chr8: 69,894,553-72,597,645 , GRCh38.p12 chr8: 68,982,318-71,685,410 LACTB2, LINC01603, 34 more genes
    nsv3902221copy number variation2nstd102humanPathogenic GRCh37 chr8: 69,899,336-72,597,645 , GRCh38.p12 chr8: 68,987,101-71,685,410 LACTB2, LACTB2-AS1, 34 more genes
    nsv3912623copy number variation1nstd102humanPathogenic GRCh37 chr8: 69,900,070-72,575,701 , NCBI36 chr8: 70,062,624-72,738,255 , GRCh38 chr8: 68,987,835-71,663,466 LACTB2, TRE-CTC14-1, 34 more genes
    nsv3921799copy number variation1nstd102humanPathogenic NCBI36 chr8: 70,062,670-72,714,817 , GRCh38 chr8: 68,987,881-71,640,028 , GRCh37 chr8: 69,900,116-72,552,263 LACTB2, LOC105375889, 34 more genes
    nsv3895923copy number variation1nstd102humanPathogenic GRCh37 chr8: 69,955,127-72,552,241 , GRCh38.p12 chr8: 69,042,892-71,640,006 LACTB2, TPM4P3, 34 more genes
    nsv3915173copy number variation1nstd102humanPathogenic NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636 LACTB2, RN7SL474P, 2109 more genes
    nsv3901821copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028 LACTB2, TBC1D31, 2109 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LACTB2, LOC101929488, 2105 more genes
    nsv3916777copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575 LACTB2, RPL5P22, 2105 more genes
    nsv3898123copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385 LACTB2, SPAG1, 2105 more genes
    nsv3908608copy number variation1nstd102humanPathogenic GRCh37 chr8: 164,984-146,293,414 , GRCh38.p12 chr8: 214,984-145,068,028 LACTB2, LINC01617, 2105 more genes
    nsv3893757copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,991-146,280,828 , GRCh38.p12 chr8: 208,991-145,055,442 LACTB2, LOC105375890, 2105 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 LACTB2, LOC112268023, 2105 more genes
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