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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5700877mobile element insertion2nstd211human GRCh38 chr9: 105,525,792-105,525,792 , GRCh37.p13 chr9: 108,288,073-108,288,073 RALGAPA1P1, FSD1L
    nsv5411484mobile element insertion1nstd206human GRCh38 chr9: 105,525,792-105,525,843 , GRCh37.p13 chr9: 108,288,073-108,288,124 RALGAPA1P1, FSD1L
    nsv5251896copy number variation1nstd204human GRCh38.p13 chr9: 105,520,304-105,522,319 , GRCh37.p13 chr9: 108,282,585-108,284,600 FSD1L, RALGAPA1P1
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4982991copy number variation1nstd200human GRCh38 chr9: 105,519,786-105,523,157 , GRCh37.p13 chr9: 108,282,067-108,285,438 FSD1L, RALGAPA1P1
    nsv4982990copy number variation1nstd200human GRCh38 chr9: 105,514,414-105,518,153 , GRCh37.p13 chr9: 108,276,695-108,280,434 RALGAPA1P1, FSD1L
    nsv4982989copy number variation1nstd200human GRCh38 chr9: 105,436,905-105,538,927 , GRCh37.p13 chr9: 108,199,186-108,301,208 FSD1L, RALGAPA1P1, 1 more genes
    nsv4834802copy number variation1nstd200human GRCh37 chr9: 108,282,067-108,285,438 , GRCh38.p12 chr9: 105,519,786-105,523,157 RALGAPA1P1, FSD1L
    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
    nsv4496101mobile element insertion1nstd166human GRCh37.p13 chr9: 108,288,067-108,288,067 , GRCh38.p12 chr9: 105,525,786-105,525,786 RALGAPA1P1, FSD1L
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 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
    nsv4185781copy number variation1nstd166human GRCh37.p13 chr9: 108,277,000-108,284,000 , GRCh38.p12 chr9: 105,514,719-105,521,719 RALGAPA1P1, FSD1L
    nsv3957795copy number variation1nstd168human GRCh38 chr9: 105,520,665-105,540,357 , GRCh37.p13 chr9: 108,282,946-108,302,638 RALGAPA1P1, FSD1L
    nsv3922729copy number variation1nstd102humanUncertain significance GRCh37 chr9: 107,572,465-110,236,202 , GRCh38 chr9: 104,810,184-107,473,921 , NCBI36 chr9: 106,612,286-109,276,023 ABCA1, LOC105376196, 34 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
    nsv3922633copy number variation2nstd102humanPathogenic GRCh38 chr9: 99,138,048-115,011,033 , NCBI36 chr9: 100,940,151-116,813,133 , GRCh37 chr9: 101,900,330-117,773,312 RAD23B, RNU6-432P, 262 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
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