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