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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5909992copy number variation1nstd209human GRCh38 chr10: 72,964,663-80,533,256 , GRCh37.p13 chr10: 74,724,421-82,293,012 , PRXL2A, 155 more genes
    nsv5867252copy number variation1nstd209human GRCh38 chr10: 79,534,832-79,543,438 , GRCh37.p13 chr10: 81,294,588-81,303,194 RPS12P18
    nsv5672415inversion1nstd207human GRCh38 chr10: 79,542,902-80,213,948 , GRCh37.p13 chr10: 81,302,658-81,973,704 , ANXA11, 30 more genes
    nsv5563886sequence alteration1nstd206human GRCh38 chr10: 79,543,104-80,217,086 , GRCh37.p13 chr10: 81,302,860-81,976,842 , ANXA11, 30 more genes
    nsv5490564copy number variation1nstd206human GRCh38 chr10: 79,534,368-79,550,368 , GRCh37.p13 chr10: 81,294,124-81,310,124 RPS12P18
    nsv5476976copy number variation1nstd206human GRCh38 chr10: 79,532,368-79,679,000 , GRCh37.p13 chr10: 81,292,124-81,438,756 MBL3P, SFTPA1, 5 more genes
    nsv5475699copy number variation1nstd206human GRCh38 chr10: 79,534,368-79,678,368 , GRCh37.p13 chr10: 81,294,124-81,438,124 MBL3P, SFTPA1, 5 more genes
    nsv5259846copy number variation1nstd204human GRCh37.p13 chr10: 81,294,657-81,420,056 , GRCh38.p13 chr10: 79,534,901-79,660,300 MBL3P, SFTPA1, 4 more genes
    nsv5250808copy number variation1nstd204human GRCh37.p13 chr10: 81,292,757-81,439,056 , GRCh38.p13 chr10: 79,533,001-79,679,300 MBL3P, SFTPA1, 5 more genes
    nsv5247790copy number variation1nstd204human GRCh38.p13 chr10: 79,533,629-79,588,377 , GRCh37.p13 chr10: 81,293,385-81,348,133 MBL3P, SFTPA2, 1 more genes
    nsv5246781copy number variation1nstd204human GRCh38.p13 chr10: 79,532,327-79,570,840 , GRCh37.p13 chr10: 81,292,083-81,330,596 SFTPA2, RPS12P18
    nsv5246384copy number variation1nstd204human GRCh38.p13 chr10: 79,534,199-79,559,637 , GRCh37.p13 chr10: 81,293,955-81,319,393 SFTPA2, RPS12P18
    nsv5244603copy number variation1nstd204human GRCh38.p13 chr10: 79,533,090-79,544,827 , GRCh37.p13 chr10: 81,292,846-81,304,583 RPS12P18
    nsv5242330copy number variation1nstd204human GRCh38.p13 chr10: 79,537,796-79,565,790 , GRCh37.p13 chr10: 81,297,552-81,325,546 SFTPA2, RPS12P18
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4729182copy number variation1nstd102humanUncertain significance GRCh37 chr10: 81,028,088-82,059,110 , GRCh38.p12 chr10: 79,268,331-80,299,354 SFTPA1, RPS12P18, 40 more genes
    nsv4682723copy number variation1nstd102humanPathogenic GRCh37 chr10: 80,961,390-81,319,734 , GRCh38.p12 chr10: 79,201,633-79,559,978 PPIF, ZMIZ1, 7 more genes
    nsv4528296copy number variation1nstd166human GRCh37.p13 chr10: 81,293,999-81,439,000 , GRCh38.p12 chr10: 79,534,243-79,679,244 MBL3P, SFTPA1, 5 more genes
    nsv4456105copy number variation1nstd102humanUncertain significance GRCh37 chr10: 81,297,994-81,422,268 , GRCh38.p12 chr10: 79,538,238-79,662,512 RPS12P18, SFTPA3P, 4 more genes
    nsv4418553copy number variation1nstd174human GRCh37 chr10: 81,251,577-81,557,993 , GRCh38.p12 chr10: 79,491,821-79,798,237 , LOC729815, 12 more genes
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