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Items: 1 to 20 of 266

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099216copy number variation1nstd231human GRCh38.p12 chr1: 94,020,799-94,715,227 , GRCh37 chr1: 94,486,355-95,180,783 ABCA4, F3, 12 more genes
    nsv7099215copy number variation1nstd231human GRCh38.p12 chr1: 84,991,383-97,594,649 , GRCh37 chr1: 85,457,066-98,060,205 ABCA4, BRDT, 220 more genes
    nsv7044428inversion1nstd229human GRCh38 chr1: 93,904,930-94,557,074 , GRCh37.p13 chr1: 94,370,486-95,022,630 MTATP6P13, MIR12133, 16 more genes
    nsv7043112inversion1nstd229human GRCh38 chr1: 94,294,099-94,296,397 , GRCh37.p13 chr1: 94,759,655-94,761,953 ARHGAP29-AS1
    nsv6657566copy number variation1nstd229human GRCh38 chr1: 94,330,206-94,343,419 , GRCh37.p13 chr1: 94,795,762-94,808,975 ARHGAP29-AS1
    nsv6657565copy number variation1nstd229human GRCh38 chr1: 94,304,196-94,304,358 , GRCh37.p13 chr1: 94,769,752-94,769,914 ARHGAP29-AS1
    nsv6657563copy number variation1nstd229human GRCh38 chr1: 94,258,401-94,270,200 , GRCh37.p13 chr1: 94,723,957-94,735,756 ARHGAP29-AS1, ARHGAP29
    nsv6657562copy number variation1nstd229human GRCh38 chr1: 94,243,289-94,250,117 , GRCh37.p13 chr1: 94,708,845-94,715,673 ARHGAP29, ARHGAP29-AS1
    nsv6657471copy number variation1nstd229human GRCh38 chr1: 94,259,496-94,269,810 , GRCh37.p13 chr1: 94,725,052-94,735,366 ARHGAP29, ARHGAP29-AS1
    nsv6657470copy number variation1nstd229human GRCh38 chr1: 94,253,864-94,263,882 , GRCh37.p13 chr1: 94,719,420-94,729,438 ARHGAP29, ARHGAP29-AS1
    nsv6657458copy number variation1nstd229human GRCh38 chr1: 93,845,890-94,640,318 , GRCh37.p13 chr1: 94,311,446-95,105,874 MIR12133, CHCHD2P5, 22 more genes
    nsv6657409copy number variation1nstd229human GRCh38 chr1: 94,301,599-94,386,193 , GRCh37.p13 chr1: 94,767,155-94,851,749 GAPDHP29, ARHGAP29-AS1
    nsv6657408copy number variation1nstd229human GRCh38 chr1: 94,296,076-94,302,355 , GRCh37.p13 chr1: 94,761,632-94,767,911 GAPDHP29, ARHGAP29-AS1
    nsv6657407copy number variation1nstd229human GRCh38 chr1: 94,265,426-94,267,623 , GRCh37.p13 chr1: 94,730,982-94,733,179 ARHGAP29, ARHGAP29-AS1
    nsv6656681copy number variation1nstd229human GRCh38 chr1: 94,295,121-94,305,319 , GRCh37.p13 chr1: 94,760,677-94,770,875 GAPDHP29, ARHGAP29-AS1
    nsv6656679copy number variation1nstd229human GRCh38 chr1: 94,268,568-94,269,076 , GRCh37.p13 chr1: 94,734,124-94,734,632 ARHGAP29, ARHGAP29-AS1
    nsv6547561inversion1nstd223human GRCh38 chr1: 94,256,857-94,257,283 , GRCh37.p13 chr1: 94,722,413-94,722,839 ARHGAP29, ARHGAP29-AS1
    nsv6335182copy number variation1nstd223human GRCh38 chr1: 94,310,961-94,311,299 , GRCh37.p13 chr1: 94,776,517-94,776,855 ARHGAP29-AS1
    nsv6334174copy number variation1nstd223human GRCh38 chr1: 94,265,426-94,267,623 , GRCh37.p13 chr1: 94,730,982-94,733,179 ARHGAP29, ARHGAP29-AS1
    nsv6332578copy number variation1nstd223human GRCh38 chr1: 94,316,529-94,317,301 , GRCh37.p13 chr1: 94,782,085-94,782,857 ARHGAP29-AS1
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