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Items: 1 to 20 of 82

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3077189copy number variation1estd209human GRCh37 chr5: 159,486,200-159,486,201 , GRCh38.p12 chr5: 160,059,193-160,059,194 PWWP2A, TTC1
    nsv949073copy number variation1nstd85human NCBI35 chr5: 152,342,899-170,989,470 , GRCh37.p13 chr5: 152,362,706-171,056,865 , GRCh38.p12 chr5: 152,983,146-171,629,861 , ADRA1B, 213 more genes
    esv2730972copy number variation1estd201human GRCh37 chr5: 159,474,197-159,474,734 , GRCh38.p12 chr5: 160,047,190-160,047,727 TTC1, PWWP2A
    esv2671720copy number variation1estd199human GRCh37 chr5: 159,529,915-159,535,432 , GRCh38.p12 chr5: 160,102,908-160,108,425 PWWP2A
    esv2662749copy number variation3estd199human GRCh37 chr5: 159,474,049-159,474,810 , GRCh38.p12 chr5: 160,047,042-160,047,803 PWWP2A, TTC1
    esv1742403copy number variation1estd22human NCBI36 chr5: 159,472,754-159,472,755 , GRCh37.p13 chr5: 159,540,176-159,540,177 , GRCh38.p12 chr5: 160,113,169-160,113,170 PWWP2A
    esv1733274copy number variation1estd22human NCBI36 chr5: 159,455,294-159,455,295 , GRCh37.p13 chr5: 159,522,716-159,522,717 , GRCh38.p12 chr5: 160,095,709-160,095,710 PWWP2A
    esv1721633insertion1estd22human NCBI36 chr5: 159,412,159-159,412,159 , GRCh37.p13 chr5: 159,479,581-159,479,581 , GRCh38.p12 chr5: 160,052,574-160,052,574 PWWP2A, TTC1
    esv1719510insertion1estd22human NCBI36 chr5: 159,451,611-159,451,611 , GRCh37.p13 chr5: 159,519,033-159,519,033 , GRCh38.p12 chr5: 160,092,026-160,092,026 PWWP2A
    esv1679351insertion1estd22human NCBI36 chr5: 159,463,725-159,463,725 , GRCh37.p13 chr5: 159,531,147-159,531,147 , GRCh38.p12 chr5: 160,104,140-160,104,140 PWWP2A
    esv1629664insertion1estd22human NCBI36 chr5: 159,461,252-159,461,252 , GRCh37.p13 chr5: 159,528,674-159,528,674 , GRCh38.p12 chr5: 160,101,667-160,101,667 PWWP2A
    esv1617536copy number variation1estd22human NCBI36 chr5: 159,435,276-159,435,278 , GRCh37.p13 chr5: 159,502,698-159,502,700 , GRCh38.p12 chr5: 160,075,691-160,075,693 PWWP2A
    esv1613995insertion1estd22human NCBI36 chr5: 159,454,662-159,454,662 , GRCh37.p13 chr5: 159,522,084-159,522,084 , GRCh38.p12 chr5: 160,095,077-160,095,077 PWWP2A
    esv1596095insertion1estd22human NCBI36 chr5: 159,411,978-159,411,978 , GRCh37.p13 chr5: 159,479,400-159,479,400 , GRCh38.p12 chr5: 160,052,393-160,052,393 TTC1, PWWP2A
    esv1590653copy number variation1estd22human NCBI36 chr5: 159,442,042-159,442,043 , GRCh37.p13 chr5: 159,509,464-159,509,465 , GRCh38.p12 chr5: 160,082,457-160,082,458 PWWP2A
    esv1585861copy number variation1estd22human NCBI36 chr5: 159,418,781-159,418,782 , GRCh37.p13 chr5: 159,486,203-159,486,204 , GRCh38.p12 chr5: 160,059,196-160,059,197 TTC1, PWWP2A
    esv1582892insertion1estd22human NCBI36 chr5: 159,410,574-159,410,574 , GRCh37.p13 chr5: 159,477,996-159,477,996 , GRCh38.p12 chr5: 160,050,989-160,050,989 PWWP2A, TTC1
    esv1582772copy number variation1estd22human NCBI36 chr5: 159,469,357-159,469,362 , GRCh37.p13 chr5: 159,536,779-159,536,784 , GRCh38.p12 chr5: 160,109,772-160,109,777 PWWP2A
    esv1577593insertion1estd22human NCBI36 chr5: 159,434,050-159,434,050 , GRCh37.p13 chr5: 159,501,472-159,501,472 , GRCh38.p12 chr5: 160,074,465-160,074,465 PWWP2A
    esv1568037copy number variation1estd22human NCBI36 chr5: 159,408,545-159,408,546 , GRCh37.p13 chr5: 159,475,967-159,475,968 , GRCh38.p12 chr5: 160,048,960-160,048,961 PWWP2A, TTC1
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