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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140092copy number variation1nstd232human GRCh37.p13 chr9: 139,327,527-139,327,605 , GRCh38.p12 chr9: 136,433,075-136,433,153 INPP5E
    nsv7139587copy number variation1nstd232human GRCh37.p13 chr9: 139,325,695-139,325,902 , GRCh38.p12 chr9: 136,431,243-136,431,450 INPP5E
    nsv7098439copy number variation1nstd102humanUncertain significance GRCh37 chr9: 139,258,754-139,325,589 , GRCh38.p12 chr9: 136,364,302-136,431,137 SNAPC4, PMPCA, 3 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
    nsv7098066copy number variation4nstd102humanUncertain significance GRCh37 chr9: 135,139,626-140,034,216 , GRCh38.p12 chr9: 132,264,239-137,139,764 LINC02692, SNORD141A, 181 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
    nsv7093414copy number variation1nstd102humanPathogenic GRCh38 chr9: 134,932,722-137,269,957 , GRCh37.p13 chr9: 137,824,568-140,164,409 LHX3, FUT7, 121 more genes
    nsv7077226inversion1nstd229human GRCh38 chr9: 136,316,295-136,475,130 , GRCh37.p13 chr9: 139,252,829-139,369,582 ENTR1, GPSM1, 7 more genes
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv7075196inversion1nstd229human GRCh38 chr9: 130,990,409-137,053,229 , GRCh37.p13 chr9: 133,865,796-139,947,681 LINC02907, LCN1, 196 more genes
    nsv7070027inversion1nstd229human GRCh38 chr9: 135,876,745-136,834,735 , GRCh37.p13 chr9: 138,768,591-139,729,187 LOC107987142, LCN8, 48 more genes
    nsv7069792inversion1nstd229human GRCh38 chr9: 136,285,122-136,523,179 , GRCh37.p13 chr9: 139,252,829-139,417,631 NOTCH1, DKFZP434A062, 11 more genes
    nsv7059760inversion1nstd229human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 LCN10, RAPGEF1, 196 more genes
    nsv7058128inversion1nstd229human GRCh38 chr9: 136,404,238-136,577,692 , GRCh37.p13 chr9: 139,298,690-139,472,144 NOTCH1, INPP5E, 7 more genes
    nsv6895385copy number variation1nstd229human GRCh38 chr9: 136,433,901-136,458,500 , GRCh37.p13 chr9: 139,328,353-139,352,952 SEC16A, INPP5E
    nsv6892503copy number variation1nstd229human GRCh38 chr9: 136,371,112-136,438,675 , GRCh37.p13 chr9: 139,265,564-139,333,127 SEC16A, PMPCA, 4 more genes
    nsv6887498copy number variation1nstd229human GRCh38 chr9: 136,214,667-136,443,437 , GRCh37.p13 chr9: 139,106,513-139,337,889 DKFZP434A062, QSOX2, 9 more genes
    nsv6885034copy number variation1nstd229human GRCh38 chr9: 136,436,260-136,463,988 , GRCh37.p13 chr9: 139,330,712-139,358,440 SEC16A, INPP5E
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