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Items: 1 to 20 of 1706

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137758copy number variation1nstd102humanUncertain significance GRCh37 chr7: 151,993,317-152,093,215 , GRCh38.p12 chr7: 152,296,232-152,396,130 KMT2C, SEPTIN7P6
    nsv6117139copy number variation1nstd186human GRCh37 chr7: 151,968,038-151,976,988 , GRCh38.p12 chr7: 152,270,953-152,279,903 KMT2C
    nsv6115354copy number variation1nstd186human GRCh37 chr7: 152,104,754-152,113,727 , GRCh38.p12 chr7: 152,407,669-152,416,642 KMT2C
    nsv6112689copy number variation1nstd102humanUncertain significance GRCh38 chr7: 152,175,569-152,524,553 , GRCh37.p13 chr7: 151,872,654-152,221,638 CCT8L1P, LINC01003, 3 more genes
    nsv5979093inversion1nstd209human GRCh38 chr7: 150,023,235-154,074,108 , GRCh37.p13 chr7: 149,720,324-153,771,193 , AOC1, 98 more genes
    nsv5956581insertion1nstd209human GRCh38 chr7: 152,215,688-152,215,688 , GRCh37.p13 chr7: 151,912,773-151,912,773 KMT2C
    nsv5955249insertion1nstd209human GRCh38 chr7: 152,385,325-152,385,325 , GRCh37.p13 chr7: 152,082,410-152,082,410 KMT2C
    nsv5918443copy number variation1nstd209human GRCh38 chr7: 152,385,313-152,385,643 , GRCh37.p13 chr7: 152,082,398-152,082,728 KMT2C
    nsv5917501copy number variation1nstd209human GRCh38 chr7: 152,320,452-152,325,351 , GRCh37.p13 chr7: 152,017,537-152,022,436 KMT2C
    nsv5915855copy number variation1nstd209human GRCh38 chr7: 152,297,031-152,297,080 , GRCh37.p13 chr7: 151,994,116-151,994,165 KMT2C
    nsv5912952copy number variation1nstd209human GRCh38 chr7: 152,388,077-152,388,129 , GRCh37.p13 chr7: 152,085,162-152,085,214 KMT2C
    nsv5908247copy number variation1nstd209human GRCh38 chr7: 152,412,062-152,412,205 , GRCh37.p13 chr7: 152,109,147-152,109,290 KMT2C
    nsv5863755copy number variation1nstd209human GRCh38 chr7: 152,238,778-152,259,034 , GRCh37.p13 chr7: 151,935,863-151,956,119 KMT2C
    nsv5863725copy number variation1nstd209human GRCh38 chr7: 152,372,768-152,374,245 , GRCh37.p13 chr7: 152,069,853-152,071,330 KMT2C
    nsv5854358copy number variation1nstd209human GRCh38 chr7: 152,144,867-152,146,966 , GRCh37.p13 chr7: 151,841,952-151,844,051 KMT2C
    nsv5851705copy number variation1nstd209human GRCh38 chr7: 152,146,017-152,160,468 , GRCh37.p13 chr7: 151,843,102-151,857,553 KMT2C
    nsv5848221copy number variation1nstd209human GRCh38 chr7: 152,320,185-152,325,312 , GRCh37.p13 chr7: 152,017,270-152,022,397 KMT2C
    nsv5848105copy number variation1nstd209human GRCh38 chr7: 152,211,880-152,234,911 , GRCh37.p13 chr7: 151,908,965-151,931,996 KMT2C
    nsv5847602copy number variation1nstd209human GRCh38 chr7: 152,155,776-152,157,518 , GRCh37.p13 chr7: 151,852,861-151,854,603 KMT2C
    nsv5725106mobile element insertion2nstd211human GRCh38 chr7: 152,171,039-152,171,039 , GRCh37.p13 chr7: 151,868,124-151,868,124 KMT2C
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