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Items: 1 to 20 of 407

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094603copy number variation1nstd102humanUncertain significance GRCh37 chr16: 83,932,750-84,211,465 , GRCh38.p12 chr16: 83,899,145-84,177,859 NECAB2, HSDL1, 9 more genes
    nsv7076578inversion1nstd229human GRCh38 chr16: 83,742,713-84,033,267 , GRCh37.p13 chr16: 83,776,318-84,066,872 HSBP1, NECAB2, 6 more genes
    nsv7076150inversion1nstd229human GRCh38 chr16: 83,426,720-84,571,834 , GRCh37.p13 chr16: 83,460,325-84,605,440 , LOC648774, 23 more genes
    nsv7073806inversion1nstd229human GRCh38 chr16: 83,959,188-84,022,126 , GRCh37.p13 chr16: 83,992,793-84,055,731 SLC38A8, OSGIN1, 1 more genes
    nsv7073024inversion1nstd229human GRCh38 chr16: 83,998,685-84,003,336 , GRCh37.p13 chr16: 84,032,290-84,036,941 NECAB2
    nsv7070244inversion1nstd229human GRCh38 chr16: 83,984,969-83,999,287 , GRCh37.p13 chr16: 84,018,574-84,032,892 NECAB2
    nsv7069912inversion1nstd229human GRCh38 chr16: 83,979,480-83,999,291 , GRCh37.p13 chr16: 84,013,085-84,032,896 NECAB2
    nsv7069513inversion1nstd229human GRCh38 chr16: 83,832,179-84,528,985 , GRCh37.p13 chr16: 83,865,784-84,562,591 HSDL1, ATP2C2-AS1, 17 more genes
    nsv6997369copy number variation1nstd229human GRCh38 chr16: 83,974,611-83,979,226 , GRCh37.p13 chr16: 84,008,216-84,012,831 NECAB2
    nsv6996807copy number variation1nstd229human GRCh38 chr16: 83,968,966-83,980,995 , GRCh37.p13 chr16: 84,002,571-84,014,600 NECAB2
    nsv6996629copy number variation1nstd229human GRCh38 chr16: 83,971,303-83,981,898 , GRCh37.p13 chr16: 84,004,908-84,015,503 NECAB2
    nsv6995823copy number variation1nstd229human GRCh38 chr16: 83,974,276-83,993,057 , GRCh37.p13 chr16: 84,007,881-84,026,662 NECAB2
    nsv6995486copy number variation1nstd229human GRCh38 chr16: 83,985,366-83,999,488 , GRCh37.p13 chr16: 84,018,971-84,033,093 NECAB2
    nsv6995142copy number variation1nstd229human GRCh38 chr16: 83,870,301-84,028,700 , GRCh37.p13 chr16: 83,903,906-84,062,305 SLC38A8, MLYCD, 3 more genes
    nsv6994608copy number variation1nstd229human GRCh38 chr16: 76,392,054-84,158,971 , GRCh37.p13 chr16: 76,425,951-84,192,576 , MAFTRR, 87 more genes
    nsv6993903copy number variation1nstd229human GRCh38 chr16: 83,896,130-84,027,702 , GRCh37.p13 chr16: 83,929,735-84,061,307 MLYCD, NECAB2, 3 more genes
    nsv6993366copy number variation1nstd229human GRCh38 chr16: 83,978,543-83,980,579 , GRCh37.p13 chr16: 84,012,148-84,014,184 NECAB2
    nsv6992668copy number variation1nstd229human GRCh38 chr16: 83,866,843-84,024,110 , GRCh37.p13 chr16: 83,900,448-84,057,715 SLC38A8, MLYCD, 3 more genes
    nsv6992485copy number variation1nstd229human GRCh38 chr16: 83,920,050-84,036,257 , GRCh37.p13 chr16: 83,953,655-84,069,862 SLC38A8, MLYCD, 3 more genes
    nsv6992361copy number variation1nstd229human GRCh38 chr16: 83,854,864-84,034,304 , GRCh37.p13 chr16: 83,888,469-84,067,909 LOC105371372, OSGIN1, 3 more genes
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