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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv959617copy number variation1nstd86human GRCh38.p12 chr6: 128,089,688-128,397,690 , GRCh37 chr6: 128,410,833-128,718,835 , GRCh38.p12 chr6|NT_187556.1: 439,022-747,024 PTPRK
    nsv958971copy number variation1nstd86human GRCh37 chr7: 48,308,577-48,545,986 , GRCh38.p12 chr7: 48,268,980-48,506,390 ABCA13
    nsv959878copy number variation1nstd86human GRCh38.p12 chr4: 161,759,409-161,920,654 , GRCh37 chr4: 162,680,561-162,841,806 FSTL5
    nsv959777copy number variation1nstd86human GRCh37 chr20: 40,944,361-41,076,971 , GRCh38.p12 chr20: 42,315,721-42,448,331 PTPRT
    nsv959023copy number variation1nstd86human GRCh37 chr3: 57,994,290-58,118,660 , GRCh38.p12 chr3: 58,008,563-58,132,933 FLNB
    nsv959686copy number variation1nstd86human GRCh38.p12 chr6: 151,009,817-151,092,558 , GRCh37 chr6: 151,330,953-151,413,694 MTHFD1L
    nsv959480copy number variation1nstd86human GRCh37 chr7: 11,513,961-11,582,744 , GRCh38.p12 chr7: 11,474,334-11,543,117 THSD7A
    nsv959382copy number variation1nstd86human GRCh38.p12 chr6: 97,178,441-97,246,692 , GRCh37 chr6: 97,626,317-97,694,568 MMS22L
    nsv958905copy number variation1nstd86human GRCh38.p12 chr1: 174,637,373-174,702,258 , GRCh37 chr1: 174,606,511-174,671,396 RABGAP1L
    nsv959610copy number variation1nstd86human GRCh37 chr18: 3,135,545-3,193,956 , GRCh38.p12 chr18: 3,135,547-3,193,958 MYOM1
    nsv959800copy number variation1nstd86human GRCh37 chr18: 30,873,121-30,928,941 , GRCh38.p12 chr18: 33,293,157-33,348,977 CCDC178
    nsv959342copy number variation1nstd86human GRCh37 chr3: 41,705,096-41,759,355 , GRCh38.p12 chr3: 41,663,605-41,717,863 ULK4
    nsv959503copy number variation6nstd86human GRCh38.p12 chr8: 16,110,083-16,164,253 , GRCh37 chr8: 15,967,592-16,021,762 MSR1
    nsv959201copy number variation1nstd86human GRCh38.p12 chr9: 15,172,017-15,226,014 , GRCh37 chr9: 15,172,015-15,226,012 TTC39B
    nsv959017copy number variation1nstd86human GRCh38.p12 chr4: 74,174,535-74,225,396 , GRCh37 chr4: 75,040,252-75,091,113 MTHFD2L
    nsv959769copy number variation1nstd86human GRCh37 chr11: 43,772,459-43,819,979 , GRCh38.p12 chr11: 43,750,909-43,798,429 HSD17B12
    nsv959697copy number variation1nstd86human GRCh37 chr7: 133,859,306-133,906,672 , GRCh38.p12 chr7: 134,174,554-134,221,920 LRGUK
    nsv959353copy number variation1nstd86human GRCh37 chr3: 102,153,957-102,196,464 , GRCh38.p12 chr3: 102,435,113-102,477,620 ZPLD1
    nsv958982copy number variation1nstd86human GRCh37 chr11: 31,086,016-31,128,507 , GRCh38.p12 chr11: 31,064,469-31,106,960 DCDC1
    nsv959910copy number variation1nstd86human GRCh37 chr3: 47,125,208-47,164,618 , GRCh38.p12 chr3: 47,083,718-47,123,128 SETD2
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