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Items: 1 to 20 of 68

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094689copy number variation1nstd102humanUncertain significance GRCh37 chr16: 70,286,624-70,305,895 , GRCh38.p12 chr16: 70,252,721-70,271,992 AARS1
    nsv6314905copy number variation1nstd102humanUncertain significance GRCh37 chr16: 70,286,624-70,293,109 , GRCh38.p12 chr16: 70,252,721-70,259,206 AARS1
    nsv6314866copy number variation1nstd102humanUncertain significance GRCh37 chr16: 70,301,542-70,305,895 , GRCh38.p12 chr16: 70,267,639-70,271,992 AARS1
    nsv4682792copy number variation1nstd102humanUncertain significance GRCh37 chr16: 70,301,552-70,305,885 , GRCh38.p12 chr16: 70,267,649-70,271,982 AARS1
    nsv4681350copy number variation1nstd102humanUncertain significance GRCh37 chr16: 70,301,552-70,302,292 , GRCh38.p12 chr16: 70,267,649-70,268,389 AARS1
    nsv3882753copy number variation1nstd102humanUncertain significance GRCh38 chr16: 70,252,701-70,262,544 , GRCh37 chr16: 70,286,604-70,296,447 AARS1
    nsv6314836copy number variation1nstd102humanUncertain significance GRCh37 chr16: 70,286,624-70,296,447 , GRCh38.p12 chr16: 70,252,721-70,262,544 AARS1
    nsv4450706copy number variation1nstd102humanUncertain significance GRCh37 chr16: 70,286,614-70,296,437 , GRCh38 chr16: 70,252,711-70,262,534 AARS1
    nsv7094593copy number variation1nstd102humanPathogenic GRCh37 chr16: 70,294,927-70,311,077 , GRCh38.p12 chr16: 70,261,024-70,277,174 AARS1, RN7SL279P
    nsv3904505copy number variation1nstd102humanBenign GRCh37 chr16: 70,284,178-70,285,129 , GRCh38.p12 chr16: 70,250,275-70,251,226 AARS1, EXOSC6
    nsv4454830copy number variation1nstd102humanUncertain significance GRCh37 chr16: 70,298,851-70,316,676 , GRCh38 chr16: 70,264,948-70,282,773 AARS1, RN7SL279P
    nsv4578659copy number variation1nstd102humanUncertain significance GRCh37 chr16: 70,305,684-70,316,666 , GRCh38.p12 chr16: 70,271,781-70,282,763 AARS1, RN7SL279P
    nsv7094594copy number variation1nstd102humanUncertain significance GRCh37 chr16: 70,310,369-70,311,077 , GRCh38.p12 chr16: 70,276,466-70,277,174 AARS1, RN7SL279P
    nsv7095040copy number variation1nstd102humanUncertain significance GRCh37 chr16: 70,286,296-70,298,860 , GRCh38.p12 chr16: 70,252,393-70,264,957 AARS1, EXOSC6
    nsv3882226copy number variation1nstd102humanUncertain significance GRCh38 chr16: 70,276,466-70,282,783 , GRCh37 chr16: 70,310,369-70,316,686 AARS1, RN7SL279P
    nsv4450175copy number variation1nstd102humanUncertain significance GRCh38 chr16: 70,276,486-70,282,763 , GRCh37 chr16: 70,310,389-70,316,666 AARS1, RN7SL279P
    nsv3900045copy number variation1nstd102humanUncertain significance GRCh37 chr16: 70,286,372-70,358,642 , GRCh38.p12 chr16: 70,252,469-70,324,739 AARS1, RN7SL279P, 2 more genes
    nsv3917504copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,951,979-76,757,245 , NCBI36 chr16: 68,509,480-75,314,746 , GRCh38 chr16: 69,918,076-76,723,348 AARS1, TRG-GCC3-1, 137 more genes
    nsv3916803copy number variation1nstd102humanPathogenic NCBI36 chr16: 68,126,727-74,517,697 , GRCh37.p13 chr16: 69,569,226-75,960,196 , GRCh38.p12 chr16: 69,535,323-75,926,298 AARS1, AP1G1, 138 more genes
    nsv6315469copy number variation1nstd102humanPathogenic GRCh37 chr16: 68,971,067-74,823,560 , GRCh38.p12 chr16: 68,937,164-74,789,662 AARS1, ZNF19, 128 more genes
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