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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4974753copy number variation1nstd200human GRCh38 chr9: 98,169,097-98,333,400 , GRCh37.p13 chr9: 100,931,379-101,095,682 CORO2A, MIR6854, 3 more genes
    nsv4814886copy number variation1nstd200human GRCh37 chr9: 100,931,378-101,095,683 , GRCh38.p12 chr9: 98,169,096-98,333,401 TBC1D2, CORO2A, 3 more genes
    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
    nsv4683944copy number variation1nstd102humanUncertain significance GRCh37 chr9: 100,190,728-101,558,793 , GRCh38.p12 chr9: 97,428,446-98,796,511 TRMO, RNU6-918P, 20 more genes
    nsv4675547copy number variation1nstd102humanUncertain significance GRCh37 chr9: 100,953,443-102,003,384 , GRCh38.p12 chr9: 98,191,161-99,241,102 SEC61B, TBC1D2, 15 more genes
    nsv4618355copy number variation1nstd183human GRCh37 chr9: 100,900,396-100,997,156 , GRCh38.p12 chr9: 98,138,114-98,234,874 LOC100131625, TBC1D2, 2 more genes
    nsv4609111copy number variation1nstd183human GRCh37 chr9: 100,904,355-100,999,144 , GRCh38.p12 chr9: 98,142,073-98,236,862 MIR6854, CORO2A, 2 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
    nsv4455320copy number variation1nstd102humanUncertain significance GRCh37 chr9: 100,936,047-101,094,912 , GRCh38.p12 chr9: 98,173,765-98,332,630 TBC1D2, GABBR2, 3 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
    nsv4455144copy number variation2nstd102humanUncertain significance GRCh37 chr9: 100,930,948-101,095,886 , GRCh38.p12 chr9: 98,168,666-98,333,604 TBC1D2, MIR6854, 3 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
    nsv4182697copy number variation1nstd166human GRCh37.p13 chr9: 100,931,379-101,095,682 , GRCh38.p12 chr9: 98,169,097-98,333,400 TBC1D2, LOC100131625, 3 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
    nsv3922551copy number variation1nstd102humanPathogenic GRCh38 chr9: 95,061,030-108,695,569 , NCBI36 chr9: 96,863,133-110,497,670 , GRCh37 chr9: 97,823,312-111,457,849 HEMGN, LOC105376183, 243 more genes
    nsv3921598copy number variation1nstd102humanPathogenic GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389 PGAP4, ECPAS, 2167 more genes
    nsv3920713copy number variation1nstd102humanPathogenic NCBI36 chr9: 193,862-140,140,210 , GRCh38 chr9: 203,862-138,125,937 , GRCh37 chr9: 203,862-141,020,389 ABHD17B, LOC100533707, 2167 more genes
    nsv3919257copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-141,073,897 , GRCh38 chr9: 204,193-138,179,445 , NCBI36 chr9: 194,193-140,193,718 LOC107987031, LOC105376234, 2169 more genes
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