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Items: 1 to 20 of 946

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142847insertion1nstd232human GRCh37.p13 chr9: 140,712,932-140,712,932 , GRCh38.p12 chr9: 137,818,480-137,818,480 EHMT1
    nsv7138903copy number variation1nstd232human GRCh37.p13 chr9: 140,713,939-140,714,052 , GRCh38.p12 chr9: 137,819,487-137,819,600 EHMT1
    nsv7098442copy number variation2nstd102humanPathogenic GRCh37 chr9: 140,646,763-140,881,326 , GRCh38.p12 chr9: 137,752,311-137,986,874 CACNA1B, EHMT1, 5 more genes
    nsv7098441copy number variation1nstd102humanPathogenic GRCh37 chr9: 140,605,399-140,729,425 , GRCh38.p12 chr9: 137,710,947-137,834,973 LOC100418938, EHMT1, 1 more genes
    nsv7098072copy number variation1nstd102humanUncertain significance GRCh37 chr9: 140,637,803-141,016,451 , GRCh38.p12 chr9: 137,743,351-138,121,999 MIR602, LOC100418938, 6 more genes
    nsv7098071copy number variation2nstd102humanPathogenic GRCh37 chr9: 139,089,171-141,016,451 , GRCh38.p12 chr9: 136,197,325-138,121,999 NPDC1, LOC101928786, 108 more genes
    nsv7098070copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr9: 138,392,557-141,016,451 , GRCh38.p12 chr9: 135,500,711-138,121,999 STPG3-AS1, CACNA1B-AS1, 132 more genes
    nsv7097938copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr9: 140,040,158-141,016,451 , GRCh38.p12 chr9: 137,145,706-138,121,999 NELFB, LOC651337, 39 more genes
    nsv7097706copy number variation1nstd102humanUncertain significance GRCh37 chr9: 140,605,399-140,729,405 , GRCh38.p12 chr9: 137,710,947-137,834,953 LOC100418938, EHMT1, 1 more genes
    nsv7097705copy number variation1nstd102humanPathogenic GRCh37 chr9: 140,513,481-140,657,292 , GRCh38.p12 chr9: 137,619,029-137,762,840 EHMT1, ARRDC1-AS1, 1 more genes
    nsv7097697copy number variation1nstd102humanUncertain significance GRCh37 chr9: 136,218,768-141,016,451 , GRCh38.p12 chr9: 133,351,913-138,121,999 LOC105376326, LOC107987143, 186 more genes
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7071557inversion1nstd229human GRCh38 chr9: 137,642,314-137,793,452 , GRCh37.p13 chr9: 140,536,766-140,687,904 LOC100418938, LOC651337, 1 more genes
    nsv7070249inversion1nstd229human GRCh38 chr9: 137,689,452-137,702,104 , GRCh37.p13 chr9: 140,583,904-140,596,556 EHMT1
    nsv7068117inversion1nstd229human GRCh38 chr9: 137,246,535-138,000,327 , GRCh37.p13 chr9: 140,140,987-140,894,779 NELFB, MIR7114, 23 more genes
    nsv7059648inversion1nstd229human GRCh38 chr9: 137,689,455-137,699,069 , GRCh37.p13 chr9: 140,583,907-140,593,521 EHMT1
    nsv6897416copy number variation1nstd229human GRCh38 chr9: 137,771,904-137,774,265 , GRCh37.p13 chr9: 140,666,356-140,668,717 EHMT1
    nsv6897048copy number variation1nstd229human GRCh38 chr9: 137,635,798-137,898,466 , GRCh37.p13 chr9: 140,530,250-140,792,918 LOC100418938, MIR602, 5 more genes
    nsv6895316copy number variation1nstd229human GRCh38 chr9: 137,835,502-137,835,560 , GRCh37.p13 chr9: 140,729,954-140,730,012 EHMT1
    nsv6895050copy number variation1nstd229human GRCh38 chr9: 137,658,107-137,666,359 , GRCh37.p13 chr9: 140,552,559-140,560,811 EHMT1
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