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Items: 1 to 20 of 227

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099244copy number variation1nstd231human GRCh38.p12 chr1: 166,864,890-169,028,321 , GRCh37 chr1: 166,834,127-168,997,559 CD247, DPT, 49 more genes
    nsv7049419inversion1nstd229human GRCh38 chr1: 167,051,242-167,052,984 , GRCh37.p13 chr1: 167,020,479-167,022,221 GPA33, LOC105371600
    nsv7041734inversion1nstd229human GRCh38 chr1: 166,263,566-167,062,529 , GRCh37.p13 chr1: 166,232,803-167,031,766 POGK, ILDR2, 16 more genes
    nsv7039884inversion1nstd229human GRCh38 chr1: 159,817,036-167,858,499 , GRCh37.p13 chr1: 159,786,826-167,827,737 TRP-AGG2-1, FCGR2C, 228 more genes
    nsv6644179copy number variation1nstd229human GRCh38 chr1: 167,066,323-167,066,658 , GRCh37.p13 chr1: 167,035,560-167,035,895 LOC105371600, GPA33
    nsv6644116copy number variation1nstd229human GRCh38 chr1: 167,079,688-167,085,153 , GRCh37.p13 chr1: 167,048,925-167,054,390 GPA33
    nsv6644115copy number variation1nstd229human GRCh38 chr1: 167,052,861-167,052,896 , GRCh37.p13 chr1: 167,022,098-167,022,133 GPA33, LOC105371600
    nsv6644009copy number variation1nstd229human GRCh38 chr1: 167,085,155-167,090,380 , GRCh37.p13 chr1: 167,054,392-167,059,617 GPA33
    nsv6644007copy number variation1nstd229human GRCh38 chr1: 167,036,449-167,051,356 , GRCh37.p13 chr1: 167,005,686-167,020,593 LOC105371600, GPA33
    nsv6643742copy number variation1nstd229human GRCh38 chr1: 167,063,540-167,063,879 , GRCh37.p13 chr1: 167,032,777-167,033,116 LOC105371600, GPA33
    nsv6540345inversion1nstd223human GRCh38 chr1: 167,051,244-167,052,984 , GRCh37.p13 chr1: 167,020,481-167,022,221 GPA33, LOC105371600
    nsv6540250inversion1nstd223human GRCh38 chr1: 163,441,141-169,028,378 , GRCh37.p13 chr1: 163,410,931-168,997,616 LOC107985452, NMNAT1P2, 96 more genes
    nsv6334522copy number variation1nstd223human GRCh38 chr1: 167,079,688-167,085,149 , GRCh37.p13 chr1: 167,048,925-167,054,386 GPA33
    nsv6333515copy number variation1nstd223human GRCh38 chr1: 167,085,155-167,090,376 , GRCh37.p13 chr1: 167,054,392-167,059,613 GPA33
    nsv6330074copy number variation1nstd223human GRCh38 chr1: 167,087,602-167,087,700 , GRCh37.p13 chr1: 167,056,839-167,056,937 GPA33
    nsv6324180copy number variation1nstd223human GRCh38 chr1: 167,087,488-167,087,953 , GRCh37.p13 chr1: 167,056,725-167,057,190 GPA33
    nsv6318033copy number variation1nstd223human GRCh38 chr1: 167,057,463-167,058,377 , GRCh37.p13 chr1: 167,026,700-167,027,614 GPA33, LOC105371600
    nsv6313719copy number variation1nstd102humanPathogenic GRCh37 chr1: 162,330,810-171,532,331 , GRCh38.p12 chr1: 162,361,020-171,563,192 LOC100420658, LOC105371610, 167 more genes
    nsv6245565mobile element insertion1nstd215human GRCh38 chr1: 167,062,667-167,062,667 , GRCh37.p13 chr1: 167,031,904-167,031,904 LOC105371600, GPA33
    nsv6133933copy number variation1nstd213human GRCh37 chr1: 161,620,000-196,730,001 , GRCh38.p12 chr1: 161,650,210-196,760,871 FASLG, SERPINC1, 510 more genes
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