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Items: 1 to 20 of 953

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148020copy number variation1nstd232human GRCh37.p13 chr9: 136,181,517-136,181,592 , GRCh38.p12 chr9: 133,306,121-133,306,196 , GRCh38.p12 chr9|NW_009646201.1: 132,215-132,290 0
    nsv7147753insertion1nstd232human GRCh37.p13 chr9: 136,182,791-136,182,791 , GRCh38.p12 chr9: 133,315,935-133,315,935 , GRCh38.p12 chr9|NW_009646201.1: 133,489-133,489 LCN1P2
    nsv7146670copy number variation1nstd232human GRCh37.p13 chr9: 136,130,667-136,130,720 , GRCh38.p12 chr9: 133,255,280-133,255,333 , GRCh38.p12 chr9|NW_009646201.1: 81,373-81,426 ABO
    nsv7145901copy number variation1nstd232human GRCh37.p13 chr9: 136,130,815-136,130,892 , GRCh38.p12 chr9: 133,255,428-133,255,505 , GRCh38.p12 chr9|NW_009646201.1: 81,521-81,598 ABO
    nsv7144293insertion1nstd232human GRCh37.p13 chr9: 136,181,469-136,181,469 , GRCh38.p12 chr9: 133,305,988-133,305,988 , GRCh38.p12 chr9|NW_009646201.1: 132,082-132,082 0
    nsv7143218insertion1nstd232human GRCh37.p13 chr9: 136,258,359-136,258,359 , GRCh38.p12 chr9: 133,392,583-133,392,583 , GRCh38.p12 chr9|NW_009646201.1: 218,677-218,677 STKLD1
    nsv7141342insertion1nstd232human GRCh37.p13 chr9: 136,200,651-136,200,651 , GRCh38.p12 chr9: 133,333,815-133,333,815 , GRCh38.p12 chr9|NW_009646201.1: 159,909-159,909 SURF6
    nsv7139486insertion1nstd232human GRCh37.p13 chr9: 136,230,635-136,230,635 , GRCh38.p12 chr9: 133,363,759-133,363,759 , GRCh38.p12 chr9|NW_009646201.1: 189,853-189,853 SURF4
    nsv7098068copy number variation1nstd102humanUncertain significance GRCh37 chr9: 136,319,517-136,324,302 , GRCh38.p12 chr9: 133,454,395-133,459,180 , GRCh38.p12 chr9|NW_009646201.1: 280,489-285,274 ADAMTS13, CACFD1
    nsv7097699copy number variation1nstd102humanPathogenic GRCh37 chr9: 136,287,564-136,291,485 , GRCh38.p12 chr9: 133,422,444-133,426,365 , GRCh38.p12 chr9|NW_009646201.1: 248,538-252,459 ADAMTS13
    nsv7097698copy number variation1nstd102humanUncertain significance GRCh37 chr9: 136,223,104-136,223,329 , GRCh38.p12 chr9|NW_009646201.1: 182,343-182,547 , GRCh38.p12 chr9: 133,356,249-133,356,453 SURF1, SURF2
    nsv6635160copy number variation1nstd227human GRCh38.p12 chr9: 133,251,881-133,256,264 , GRCh37 chr9: 136,127,268-136,131,651 , GRCh38.p12 chr9|NW_009646201.1: 77,840-82,357 ABO
    nsv6633673copy number variation1nstd224human GRCh37 chr9: 136,339,229-136,353,350 , GRCh38.p12 chr9: 133,474,107-133,488,228 , GRCh38.p12 chr9|NW_009646201.1: 300,201-314,322 SLC2A6
    nsv6633672copy number variation1nstd224human GRCh37 chr9: 136,280,025-136,291,594 , GRCh38.p12 chr9: 133,414,905-133,426,474 , GRCh38.p12 chr9|NW_009646201.1: 240,999-252,568 REXO4, ADAMTS13
    nsv6633586copy number variation1nstd224human GRCh37 chr9: 136,031,412-136,173,565 , GRCh38.p12 chr9: 133,156,025-133,297,990 , GRCh38.p12 chr9|NW_009646201.1: 1-124,084 ABO, OBP2B, 2 more genes
    nsv6308706insertion1nstd186human GRCh37 chr9: 136,097,437-136,097,487 , GRCh38.p12 chr9: 133,222,050-133,222,100 , GRCh38.p12 chr9|NW_009646201.1: 47,996-48,046 OBP2B
    nsv6308071mobile element insertion1nstd186human GRCh37 chr9: 136,093,537-136,093,575 , GRCh38.p12 chr9: 133,218,150-133,218,188 , GRCh38.p12 chr9|NW_009646201.1: 44,096-44,134 OBP2B
    nsv6305253copy number variation1nstd186human GRCh37 chr9: 136,231,602-136,231,659 , GRCh38.p12 chr9|NW_009646201.1: 190,820-190,877 , GRCh38.p12 chr9: 133,364,726-133,364,783 SURF4
    nsv6304814copy number variation1nstd186human GRCh37 chr9: 136,197,889-136,211,641 , GRCh38.p12 chr9: 133,331,053-133,344,786 , GRCh38.p12 chr9|NW_009646201.1: 157,147-170,880 MED22, SURF6, 1 more genes
    nsv6304575copy number variation1nstd186human GRCh37 chr9: 136,170,730-136,176,710 , GRCh38.p12 chr9: 133,295,158-133,301,227 , GRCh38.p12 chr9|NW_009646201.1: 121,252-127,321 0
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