Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv508947 | Chr1:16909817 - 17011115 on Build GRCh38 | Insertion | ATP13A2 MFAP2 CROCC |
nsv954854 | Chr1:16961106 - 17013905 on Build GRCh38 | Deletion | ATP13A2 MFAP2 CROCC |
nsv428421 | Chr1:16437838 - 17157486 on Build GRCh38 | Gain+Loss | CROCCP3 LOC105376805 RNU1-4 MST1P2 RNU1-3 LOC100132147 FAM231A SPATA21 LOC105376796 ESPNP SDHB PADI2 ATP13A2 RNU1-1 MST1L NBPF1 RNU1-2 FAM231B MFAP2 LOC102723383 MIR3675 NECAP2 CROCC CROCCP2 |
dgv108n100 | Chr1:16850538 - 17010370 on Build GRCh38 | Gain | LOC105376805 ATP13A2 RNU1-2 MFAP2 MIR3675 CROCC |
dgv92n100 | Chr1:16684943 - 17003642 on Build GRCh38 | Gain | LOC105376805 ATP13A2 RNU1-4 MST1L RNU1-2 MFAP2 LOC102723383 MIR3675 CROCC ESPNP |
nsv834280 | Chr1:16888218 - 17123006 on Build GRCh38 | Loss | PADI2 LOC105376805 ATP13A2 RNU1-2 MFAP2 CROCC SDHB |
dgv120n100 | Chr1:16890896 - 16997938 on Build GRCh38 | Gain | ATP13A2 RNU1-2 MFAP2 CROCC |
nsv834269 | Chr1:16855283 - 17038531 on Build GRCh38 | Loss | LOC105376805 ATP13A2 RNU1-2 MFAP2 MIR3675 CROCC SDHB |