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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097901copy number variation1nstd102humanUncertain significance GRCh37 chr8: 25,276,935-25,276,996 , GRCh38.p12 chr8: 25,419,419-25,419,480 GNRH1
    nsv3894721copy number variation1nstd102humanUncertain significance GRCh37 chr8: 25,276,770-25,315,893 , GRCh38.p12 chr8: 25,419,254-25,458,377 GNRH1, KCTD9, 1 more genes
    nsv6636762copy number variation1nstd102humanUncertain significance GRCh37 chr8: 25,232,694-25,511,821 , GRCh38.p12 chr8: 25,375,178-25,654,305 GNRH1, CDCA2, 3 more genes
    nsv6315449copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940 GNRH1, 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 GNRH1, LINC03022, 472 more genes
    nsv7148146copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,721,809-30,183,737 , GRCh37.p13 chr8: 12,579,318-30,041,253 GNRH1, 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 GNRH1, 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 GNRH1, 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 GNRH1, RPLP1P9, 259 more genes
    nsv3919731copy number variation1nstd102humanPathogenic GRCh38 chr8: 25,171,103-31,750,600 , NCBI36 chr8: 25,084,535-31,727,658 , GRCh37 chr8: 25,028,618-31,608,116 GNRH1, LOC100131127, 122 more genes
    nsv3923302copy number variation1nstd102humanPathogenic GRCh38 chr8: 24,910,364-31,210,737 , NCBI36 chr8: 24,823,781-31,187,795 , GRCh37 chr8: 24,767,877-31,068,253 GNRH1, BNIP3L, 123 more genes
    nsv3911687copy number variation1nstd102humanPathogenic GRCh38 chr8: 24,910,364-31,196,357 , NCBI36 chr8: 24,823,781-31,173,415 , GRCh37 chr8: 24,767,877-31,053,873 GNRH1, EXTL3-AS1, 123 more genes
    nsv4455606copy number variation1nstd102humanPathogenic GRCh37 chr8: 22,442,548-27,369,334 , GRCh38.p12 chr8: 22,585,035-27,511,817 GNRH1, PPP2R2A, 91 more genes
    nsv4675292copy number variation1nstd102humanPathogenic GRCh37 chr8: 24,305,969-28,673,405 , GRCh38.p12 chr8: 24,448,456-28,815,888 GNRH1, LOC112268023, 79 more genes
    nsv3921037copy number variation1nstd102humanPathogenic NCBI36 chr8: 23,699,280-27,439,684 , GRCh37.p13 chr8: 23,643,335-27,383,767 , GRCh38.p12 chr8: 23,785,822-27,526,250 GNRH1, DPYSL2, 53 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 GNRH1, RN7SL474P, 2109 more genes
    nsv3901821copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028 GNRH1, TBC1D31, 2109 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 GNRH1, 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 GNRH1, RPL5P22, 2105 more genes
    nsv3898123copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385 GNRH1, SPAG1, 2105 more genes
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