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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6312635copy number variation1nstd102humanUncertain significance GRCh37 chr8: 22,262,224-22,277,211 , GRCh38.p12 chr8: 22,404,711-22,419,698 SLC39A14
    nsv4455936copy number variation1nstd102humanUncertain significance GRCh37 chr8: 22,151,127-22,225,228 , GRCh38.p12 chr8: 22,293,614-22,367,715 SLC39A14, PIWIL2
    nsv3895845copy number variation1nstd102humanLikely benign GRCh37 chr8: 22,167,513-22,332,527 , GRCh38.p12 chr8: 22,310,000-22,475,014 SLC39A14, RPL21P77, 3 more genes
    nsv3900466copy number variation1nstd102humanBenign GRCh37 chr8: 22,238,030-22,374,794 , GRCh38.p12 chr8: 22,380,517-22,517,281 SLC39A14, BTF3P3, 3 more genes
    nsv4455670copy number variation1nstd102humanUncertain significance GRCh37 chr8: 22,139,159-22,337,479 , GRCh38.p12 chr8: 22,281,646-22,479,966 SLC39A14, RNU6-336P, 3 more genes
    nsv6315449copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940 SLC39A14, LOC101928016, 568 more genes
    nsv3917350copy number variation2nstd102humanPathogenic GRCh37 chr8: 2,292,235-27,361,796 , GRCh38 chr8: 2,475,295-27,504,279 , NCBI36 chr8: 2,121,457-27,417,713 SLC39A14, LINC03022, 472 more genes
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 SLC39A14, ENTPD4, 447 more genes
    nsv7148146copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,721,809-30,183,737 , GRCh37.p13 chr8: 12,579,318-30,041,253 SLC39A14, LOC101929028, 274 more genes
    nsv3916527copy number variation1nstd102humanPathogenic NCBI36 chr8: 15,137,722-32,366,274 , GRCh37.p13 chr8: 15,093,351-32,246,732 , GRCh38.p12 chr8: 15,235,842-32,389,216 SLC39A14, LOC105379343, 281 more genes
    nsv3921296copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,383,584-29,033,946 , NCBI36 chr8: 12,285,464-28,947,382 , GRCh37 chr8: 12,241,093-28,891,463 SLC39A14, XPO7, 264 more genes
    nsv3923174copy number variation1nstd102humanPathogenic GRCh38 chr8: 18,972,996-33,619,264 , GRCh37 chr8: 18,830,506-33,476,782 , NCBI36 chr8: 18,874,786-33,596,324 SLC39A14, RPLP1P9, 259 more genes
    nsv3896830copy number variation1nstd102humanPathogenic GRCh37 chr8: 13,091,530-24,483,615 , GRCh38.p12 chr8: 13,234,021-24,626,102 SLC39A14, LOC105379297, 161 more genes
    nsv4457159copy number variation1nstd102humanPathogenic GRCh37 chr8: 21,662,847-24,199,218 , GRCh38.p12 chr8: 21,805,335-24,341,705 SLC39A14, SINHCAFP3, 66 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 SLC39A14, RN7SL474P, 2109 more genes
    nsv3901821copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028 SLC39A14, TBC1D31, 2109 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 SLC39A14, 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 SLC39A14, RPL5P22, 2105 more genes
    nsv3898123copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385 SLC39A14, SPAG1, 2105 more genes
    nsv3908608copy number variation1nstd102humanPathogenic GRCh37 chr8: 164,984-146,293,414 , GRCh38.p12 chr8: 214,984-145,068,028 SLC39A14, LINC01617, 2105 more genes
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