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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3900217copy number variation1nstd102humanUncertain significance GRCh37 chr9: 17,600,135-17,842,094 , GRCh38.p12 chr9: 17,600,137-17,842,096 SH3GL2
    nsv3897957copy number variation1nstd102humanBenign GRCh37 chr9: 17,581,039-17,657,019 , GRCh38.p12 chr9: 17,581,041-17,657,021 SH3GL2, PABPC1P11
    nsv3890068copy number variation1nstd102humanLikely benign GRCh37 chr9: 17,788,590-17,999,378 , GRCh38.p12 chr9: 17,788,592-17,999,380 SH3GL2, LOC105375987, 1 more genes
    nsv4728815copy number variation1nstd102humanLikely benign GRCh37 chr9: 17,165,697-17,708,155 , GRCh38.p12 chr9: 17,165,699-17,708,157 SH3GL2, PABPC1P11, 3 more genes
    nsv3920950copy number variation1nstd102humanPathogenic NCBI36 chr9: 194,104-18,872,279 , GRCh37 chr9: 204,104-18,882,279 , GRCh38 chr9: 204,104-18,882,281 SH3GL2, RPL4P5, 193 more genes
    nsv3910019copy number variation1nstd102humanPathogenic GRCh38 chr9: 220,253-18,708,805 , NCBI36 chr9: 210,253-18,698,803 , GRCh37 chr9: 220,253-18,708,803 SH3GL2, LOC107987049, 191 more genes
    nsv5381767copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814 SH3GL2, ACTG1P14, 191 more genes
    nsv4768366copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,073,357 , GRCh38.p12 chr9: 204,193-18,073,359 SH3GL2, DOCK8-AS1, 186 more genes
    nsv3910119copy number variation1nstd102humanPathogenic NCBI36 chr9: 194,193-18,063,357 , GRCh38 chr9: 204,193-18,073,359 , GRCh37 chr9: 204,193-18,073,357 SH3GL2, RNA5SP279, 186 more genes
    nsv3917303copy number variation1nstd102humanPathogenic GRCh38 chr9: 220,253-18,073,359 , GRCh37 chr9: 220,253-18,073,357 , NCBI36 chr9: 210,253-18,063,357 SH3GL2, DMAC1, 185 more genes
    nsv4674929copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-17,789,410 , GRCh38.p12 chr9: 203,861-17,789,412 SH3GL2, LINC02851, 184 more genes
    nsv3905168copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-17,655,298 , GRCh38.p12 chr9: 203,861-17,655,300 SH3GL2, RANBP6, 184 more genes
    nsv6315395copy number variation1nstd102humanPathogenic GRCh37 chr9: 4,992,582-19,322,101 , GRCh38.p12 chr9: 4,992,582-19,322,103 SH3GL2, FREM1, 142 more genes
    nsv3921658copy number variation1nstd102humanPathogenic GRCh38 chr9: 9,661,633-18,034,356 , GRCh37 chr9: 9,661,633-18,034,354 , NCBI36 chr9: 9,651,633-18,024,354 SH3GL2, LURAP1L, 67 more genes
    nsv3914995copy number variation1nstd102humanPathogenic GRCh37 chr9: 11,086,096-17,636,669 , NCBI36 chr9: 11,076,096-17,626,669 , GRCh38 chr9: 11,086,096-17,636,671 SH3GL2, CLCN3P1, 60 more genes
    nsv3911366copy number variation1nstd102humanPathogenic GRCh37 chr9: 11,818,291-17,963,880 , GRCh38 chr9: 11,818,291-17,963,882 , NCBI36 chr9: 11,808,291-17,953,880 SH3GL2, RN7SL98P, 59 more genes
    nsv3901600copy number variation1nstd102humanPathogenic GRCh37 chr9: 13,563,537-18,491,752 , GRCh38.p12 chr9: 13,563,538-18,491,754 SH3GL2, LOC105375983, 48 more genes
    nsv3905362copy number variation1nstd102humanPathogenic GRCh37 chr9: 13,739,630-18,023,839 , GRCh38.p12 chr9: 13,739,631-18,023,841 SH3GL2, LOC389705, 45 more genes
    nsv3912247copy number variation1nstd102humanPathogenic NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981 SH3GL2, ALOX15P2, 2184 more genes
    nsv3890420copy number variation1nstd102humanPathogenic GRCh37 chr9: 10,590-141,122,247 , GRCh38.p12 chr9: 10,590-138,231,797 SH3GL2, TBC1D13, 2183 more genes
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