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Items: 1 to 20 of 125

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5955680insertion1nstd209human GRCh38 chr9: 95,523,886-95,523,886 , GRCh37.p13 chr9: 98,286,168-98,286,168 LOC105376157
    nsv5914425copy number variation1nstd209human GRCh38 chr9: 95,527,126-95,527,178 , GRCh37.p13 chr9: 98,289,408-98,289,460 LOC105376157
    nsv5381561copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807 TBC1D2, ZNF782, 170 more genes
    nsv5317404copy number variation1nstd204human GRCh38.p13 chr9: 95,550,606-95,572,698 , GRCh37.p13 chr9: 98,312,888-98,334,980 LOC105376157
    nsv5255264copy number variation1nstd204human GRCh38.p13 chr9: 95,550,604-95,561,096 , GRCh37.p13 chr9: 98,312,886-98,323,378 LOC105376157
    nsv5130184mobile element insertion1nstd203human GRCh38 chr9: 95,537,336-95,537,348 , GRCh37.p13 chr9: 98,299,618-98,299,630 LOC105376157
    nsv4982630copy number variation1nstd200human GRCh38 chr9: 95,527,126-95,527,186 , GRCh37.p13 chr9: 98,289,408-98,289,468 LOC105376157
    nsv4974736copy number variation1nstd200human GRCh38 chr9: 95,550,616-95,572,689 , GRCh37.p13 chr9: 98,312,898-98,334,971 LOC105376157
    nsv4814872copy number variation1nstd200human GRCh37 chr9: 98,312,898-98,334,971 , GRCh38.p12 chr9: 95,550,616-95,572,689 LOC105376157
    nsv4684256copy number variation1nstd102humanPathogenic GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991 RPS26P37, MIR27B, 238 more genes
    nsv4676103copy number variation1nstd102humanPathogenic NCBI36 chr9: 95,946,863-99,986,314 , GRCh37.p13 chr9: 96,907,042-100,946,493 , GRCh38.p12 chr9: 94,144,760-98,184,211 MIR3074, LOC112268039, 108 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4456543copy number variation1nstd102humanPathogenic GRCh37 chr9: 98,156,960-99,345,624 , GRCh38.p12 chr9: 95,394,678-96,583,342 LOC105376157, LOC107987103, 26 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4184749copy number variation1nstd166human GRCh37.p13 chr9: 98,304,104-98,311,055 , GRCh38.p12 chr9: 95,541,822-95,548,773 LOC105376157
    nsv4183539copy number variation1nstd166human GRCh37.p13 chr9: 98,291,026-98,298,664 , GRCh38.p12 chr9: 95,528,744-95,536,382 LOC105376157
    nsv3922790copy number variation1nstd102humanPathogenic GRCh38 chr9: 94,713,892-98,121,186 , GRCh37 chr9: 97,476,174-100,883,468 , NCBI36 chr9: 96,515,995-99,923,289 CDC14B, PTCH1, 87 more genes
    nsv3922685copy number variation1nstd102humanPathogenic GRCh38 chr9: 88,522,292-113,687,796 , NCBI36 chr9: 90,327,027-115,489,897 , GRCh37 chr9: 91,137,207-116,450,076 MUSK, LOC105376176, 464 more genes
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
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