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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093169copy number variation1nstd102humanPathogenic GRCh37 chr3: 123,383,000-123,383,061 , GRCh38 chr3: 123,664,153-123,664,214 MYLK
    nsv3879572copy number variation1nstd102humanBenign GRCh37 chr3: 123,315,446-123,316,526 , GRCh38.p12 chr3: 123,596,599-123,597,679 MYLK-AS1
    nsv4453176copy number variation1nstd102humanUncertain significance GRCh37 chr3: 123,455,170-123,487,068 , GRCh38.p12 chr3: 123,736,323-123,768,221 MYLK
    nsv3884074copy number variation1nstd102humanUncertain significance GRCh38 chr3: 123,682,204-123,682,330 , GRCh37 chr3: 123,401,051-123,401,177 MYLK
    nsv4682537copy number variation1nstd102humanUncertain significance GRCh37 chr3: 123,401,061-123,401,167 , GRCh38.p12 chr3: 123,682,214-123,682,320 MYLK
    nsv6311771copy number variation1nstd102humanUncertain significance GRCh37 chr3: 123,401,061-123,404,712 , GRCh38.p12 chr3: 123,682,214-123,685,865 MYLK
    nsv7096438copy number variation1nstd102humanUncertain significance GRCh37 chr3: 123,401,058-123,401,181 , GRCh38.p12 chr3: 123,682,211-123,682,334 MYLK
    nsv6311950copy number variation1nstd102humanPathogenic GRCh37 chr3: 123,332,952-123,386,054 , GRCh38.p12 chr3: 123,614,105-123,667,207 MYLK, MYLK-AS1
    nsv3924157copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 125,046,009-125,101,601 , GRCh37 chr3: 123,563,319-123,618,911 , GRCh38 chr3: 123,844,472-123,900,064 MYLK, CCDC14
    nsv3884202copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 123,563,319-123,618,911 , GRCh38.p12 chr3: 123,844,472-123,900,064 MYLK, CCDC14
    nsv6311772copy number variation1nstd102humanUncertain significance GRCh37 chr3: 123,426,778-123,453,370 , GRCh38.p12 chr3: 123,707,931-123,734,523 MYLK, LOC105369194
    nsv6314308insertion1nstd102humanUncertain significance GRCh37 chr3: 123,419,168-123,419,168 , GRCh38 chr3: 123,700,321-123,700,321 MYLK, LOC105369194
    nsv3878274copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 123,477,546-123,688,038 , GRCh38.p12 chr3: 123,758,699-123,969,191 MYLK, ROPN1, 1 more genes
    nsv4728210copy number variation1nstd102humanUncertain significance GRCh37 chr3: 123,442,360-123,837,654 , GRCh38.p12 chr3: 123,723,513-124,118,807 MYLK, KALRN, 2 more genes
    nsv5564187copy number variation1nstd102humanUncertain significance GRCh37 chr3: 123,332,942-123,512,698 , GRCh38.p12 chr3: 123,614,095-123,793,851 MYLK, MYLK-AS1, 2 more genes
    nsv3882578copy number variation1nstd102humanUncertain significance GRCh37 chr3: 123,288,885-123,426,682 , GRCh38.p12 chr3: 123,570,038-123,707,835 MYLK, LOC105369194, 3 more genes
    nsv7096927copy number variation1nstd102humanPathogenic GRCh37 chr3: 123,003,455-123,512,688 , GRCh38.p12 chr3: 123,284,608-123,793,841 MYLK, ADCY5, 4 more genes
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 MYLK, NECTIN3, 418 more genes
    nsv3918094copy number variation1nstd102humanPathogenic NCBI36 chr3: 113,822,514-129,935,667 , GRCh38 chr3: 112,620,977-128,734,134 , GRCh37 chr3: 112,339,824-128,452,977 MYLK, QTRT2, 284 more genes
    nsv6311770copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,365,818-133,465,047 , GRCh38.p12 chr3: 120,646,971-133,746,203 MYLK, HNRNPA1P23, 278 more genes
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