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Items: 1 to 20 of 246

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5908230copy number variation1nstd209human GRCh38 chr7: 80,217,198-80,217,249 , GRCh37.p13 chr7: 79,846,514-79,846,565 GNAI1
    nsv5907991copy number variation1nstd209human GRCh38 chr7: 80,164,872-80,164,929 , GRCh37.p13 chr7: 79,794,188-79,794,245 GNAI1
    nsv5690917mobile element insertion1nstd211human GRCh38 chr7: 80,158,086-80,158,086 , GRCh37.p13 chr7: 79,787,402-79,787,402 GNAI1
    nsv5675038mobile element insertion1nstd211human GRCh38 chr7: 80,223,849-80,223,849 , GRCh37.p13 chr7: 79,853,165-79,853,165 GNAI1
    nsv5636836insertion1nstd207human GRCh38 chr7: 80,137,317-80,137,317 , GRCh37.p13 chr7: 79,766,633-79,766,633 GNAI1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5554578sequence alteration1nstd206human GRCh38 chr7: 79,844,202-80,389,736 , GRCh37.p13 chr7: 79,473,518-80,019,052 SNRPBP1, LOC101927269, 9 more genes
    nsv5492960copy number variation1nstd206human GRCh38 chr7: 80,164,873-80,164,930 , GRCh37.p13 chr7: 79,794,189-79,794,246 GNAI1
    nsv5490870copy number variation1nstd206human GRCh38 chr7: 80,193,476-80,193,537 , GRCh37.p13 chr7: 79,822,792-79,822,853 GNAI1
    nsv5482070copy number variation1nstd206human GRCh38 chr7: 80,179,624-80,186,013 , GRCh37.p13 chr7: 79,808,940-79,815,329 GNAI1
    nsv5405892mobile element insertion1nstd206human GRCh38 chr7: 80,158,086-80,158,137 , GRCh37.p13 chr7: 79,787,402-79,787,453 GNAI1
    nsv5399058mobile element insertion1nstd206human GRCh38 chr7: 80,223,849-80,223,900 , GRCh37.p13 chr7: 79,853,165-79,853,216 GNAI1
    nsv5363878translocation1nstd200human GRCh38 chr7: 80,184,091-80,184,091 , GRCh38 chr7: 80,182,228-80,182,228 , GRCh37.p13 chr7: 79,811,544-79,811,544 , GRCh37.p13 chr7: 79,813,407-79,813,407 GNAI1
    nsv5362411translocation1nstd200human GRCh38 chr7: 80,151,536-80,151,536 , GRCh38 chr5: 91,123,817-91,123,817 , GRCh37.p13 chr5: 90,419,634-90,419,634 , GRCh37.p13 chr7: 79,780,852-79,780,852 GNAI1, ADGRV1
    nsv5341062translocation1nstd200human GRCh37 chr7: 79,770,754-79,770,754 , GRCh37 chr7: 79,771,004-79,771,004 , GRCh38.p12 chr7: 80,141,688-80,141,688 , GRCh38.p12 chr7: 80,141,438-80,141,438 GNAI1
    nsv5255782copy number variation1nstd204human GRCh38.p13 chr7: 80,193,901-80,197,600 , GRCh37.p13 chr7: 79,823,217-79,826,916 GNAI1
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4964874copy number variation1nstd200human GRCh38 chr7: 80,179,644-80,185,993 , GRCh37.p13 chr7: 79,808,960-79,815,309 GNAI1
    nsv4950242copy number variation1nstd200human GRCh38 chr7: 80,141,438-80,141,688 , GRCh37.p13 chr7: 79,770,754-79,771,004 GNAI1
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