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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6636020copy number variation1nstd102humanPathogenic GRCh38 chr2: 11,815,241-11,824,631 , GRCh37 chr2: 11,955,367-11,964,757 LPIN1
    nsv6311336copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,959,590-11,959,744 , GRCh38.p12 chr2: 11,819,464-11,819,618 LPIN1
    nsv4682924copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,959,610-11,959,724 , GRCh38.p12 chr2: 11,819,484-11,819,598 LPIN1
    nsv6311458copy number variation1nstd102humanUncertain significance GRCh37 chr2: 11,919,625-11,945,302 , GRCh38.p12 chr2: 11,779,499-11,805,176 LPIN1
    nsv6311289copy number variation1nstd102humanUncertain significance GRCh37 chr2: 11,960,517-11,964,917 , GRCh38.p12 chr2: 11,820,391-11,824,791 LPIN1
    nsv7096195copy number variation1nstd102humanUncertain significance GRCh37 chr2: 11,923,935-11,925,222 , GRCh38.p12 chr2: 11,783,809-11,785,096 LPIN1
    nsv6311337copy number variation1nstd102humanUncertain significance GRCh37 chr2: 11,959,590-11,960,660 , GRCh38.p12 chr2: 11,819,464-11,820,534 LPIN1
    nsv7096364copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr2: 11,905,668-11,964,917 , GRCh38.p12 chr2: 11,765,542-11,824,791 LPIN1, MIR548S
    nsv6311335copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,905,668-11,955,386 , GRCh38.p12 chr2: 11,765,542-11,815,260 LPIN1, MIR548S
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 LPIN1, CYP1B1-AS1, 1649 more genes
    nsv3908896copy number variation1nstd102humanPathogenic GRCh37 chr2: 6,671,304-16,243,921 , GRCh38 chr2: 6,531,172-16,103,799 , NCBI36 chr2: 6,588,755-16,161,372 LPIN1, RNU6-1288P, 138 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LPIN1, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 LPIN1, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 LPIN1, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 LPIN1, MTND2P22, 3724 more genes
    nsv3908605copy number variation1nstd102humanPathogenic GRCh37 chr2: 66,097-55,797,773 , GRCh38 chr2: 66,097-55,570,637 , NCBI36 chr2: 56,097-55,651,277 LPIN1, SLC35F6, 801 more genes
    nsv3908288copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,816-46,210,371 , GRCh38 chr2: 236,816-45,983,232 , NCBI36 chr2: 226,816-46,063,875 LPIN1, ALLC, 674 more genes
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LPIN1, LOC105374455, 504 more genes
    nsv3908038copy number variation1nstd102humanPathogenic GRCh37 chr2: 12,770-33,936,576 , NCBI36 chr2: 2,770-33,790,080 , GRCh38 chr2: 12,770-33,711,509 LPIN1, LOC105373394, 507 more genes
    nsv3907033copy number variation1nstd102humanPathogenic NCBI36 chr2: 20,341-28,496,035 , GRCh38 chr2: 30,341-28,419,664 , GRCh37 chr2: 30,341-28,642,531 LPIN1, GTF3C2-AS1, 434 more genes
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